Recalls in November 2019

Mark Feldstein & Associates of Sylvania, Ohio, is recalling about 5,000 Stacked Gourd Jack-O-Lantern decorations.

The string light wiring inside the Jack-O-Lanterns can overheat, spark or ignite, posing a fire hazard.

The firm has received four reports of the Jack-O-Lantern decorations smoking or catching fire. No injuries or property damage are reported.

This recall involves Stacked Gourd Jack-O-Lantern decorations. The 12-inch Jack-O-Lantern is hand-painted resin and has battery-operated LED string lights inside the product.

The Jack-O-Lantern’s lights are powered with three AAA batteries. Printed on a hang tag and a label on the box is UPC code 789683062481, model number S1915D12 and Mark Feldstein & Associates Inc.

The decorations, manufactured in China, were sold at Paper Store, Hallmark stores, and independent gift stores nationwide from August 2019, through October 2019, and online at www.Amazon.com from July 2019, through September 2019, for about $20.

What to do

Consumers should immediately stop using the recalled Stacked Gourd Jack-O-Lantern decorations and contact Mark Feldstein & Associates to receive a full refund.

Consumers may contact Mark Feldstein & Associates at (800) 755-6504 from 8:15 a.m. to 5 p.m. (ET) Monday through Friday, by email at Sales@MFAgifts.com or online at www.MFAgifts.com and click on “Recall Information” at the top of the page for more information.

Golden State Medical Supply (GSMS) is recalling all quantities and lots of Ranitidine HCl 150-mg and 300-mg capsules.

The product may contain N-Nitrosodimethylamine (NDMA ), a substance that could cause cancer, above levels established by the FDA.

The firm has not received any reports of adverse events.

The following products, used for treatment of gastric disorders, are being recalled:

The lots being recalled were primarily sold to AmerisourceBergen, McKesson, and Tricare Mail Order Pharmacies (TMOP).

What to do

Patients taking the recalled products should consult with their physician, pharmacist, or healthcare provider about an alternative treatment prior to discontinuing the use of the medication.

Once an alternative treatment has been prescribed, patients should contact the recall processor at (866) 382-8606 or by email at Novitiumpharma6639@stericycle.com to obtain instructions and kit for returning the remaining product.

Consumers with questions may contact GSMS at (800) 284-8633, ext. 215 Monday through Friday from 7:30 AM to 4:00 PM (PT) by fax at (805) 437-7588 or by email at recalls@gsms.us

CHS of Inver Grove Heights, Minn., is recalling 67 tons of Payback Feeds.

The products may contain high levels of magnesium.

Excess dietary magnesium in animals could result in osmotic diarrhea and a marked decrease in feed intake and result in death.

The company has received reports of the deaths of 403 pheasants.

The following products, bagged in 50 lb. bags that display the Payback Feed brand, are being recalled:

The recalled products were distributed in Wyoming and Montana from September 9 – October 4, 2019.

What to do

Customers who purchased the recalled products should immediately stop using and return them to their local dealer or directly to CHS for full refund.

If animals that consumed the recalled products have the above symptoms, a veterinarian should be contacted.

Consumers with questions may contact the from at (406) 453-7646 from 8 a.m. – 4 p.m. (MST) Monday – Friday.

Voyager Industries is recalling 1,062 model year 2018-2020 Yetti Fish House Angler, Grand Excape and Traxx trailers.

The vehicles may be missing retainer clips at the spindle nut, potentially causing the spindle nut to loosen and fall off.

If the spindle nut loosens or falls off, the wheel may come off the axle assembly, posing the risk of a crash.

What to do

Voyager Industries will notify owners, and, if missing, dealers will install retainer clips at the spindle nut free of charge.

The recall began November 11, 2019.

Owners may contact Voyager Industries customer service at (800) 834-4940.

Nature’s Rx is recalling one lot of Silver Bullet, which is marketed as a male enhancement.

An FDA laboratory analysis found the product to contain sildenafil, a PDE-5 inhibitor not declared on the label that may pose serious health risks to consumers with underlying medical issues.

The firm has not received any reports of adverse events.

The recalled product is contained in blister foil sheets and packaged in small boxes containing 10 capsules with an expiration date of November 2022, and lot number: 01251ZX1.

It was sold on online.

What to do

Nature’s Rx is notifying its customers by replacement or refund and is arranging for return or replacement of all recalled products. Customers who purchased the recalled product should stop using it and discard or return it.

Consumers with questions may contact Nature’s Rx at (888) 925-5551 Monday – Friday from 10 AM – 6 PM (PST). By email at naturesrxsales@gmail.com, or by mail at 310 N Indian Hill Blvd Ste 600, Claremont, CA 91711

SCARPA North America of Boulder, Colo., is recalling about 5,400 Maestrale RS and Maestrale Men’s ski boots sold in the U.S., and Canada.

The ski boot shell can crack, posing a fall hazard and risk of injury to the consumer.

This recall involves the Fall 2017 Maestrale RS and Maestrale Men’s Ski Boots.

The Maestrale style numbers are #12047/501.1 and can be identified by their orange color, and the “SCARPA” name on lower-outside shell and “Maestrale” model name on upper/outside cuff.

The Maestrale RS style numbers are #12046/501.1 and can be identified by their white, black and lime color, and the “SCARPA” name on lower-outside shell and “Maestrale RS” model name on upper/outside cuff.

The boots, manufactured in Italy, were sold at authorized SCARPA dealers and outdoor stores nationwide and online at www.scarpa.com from August 2017, through August 2019, for $700 for the Maestrale model and $800 for the Maestrale RS model.

What to do

Consumers should immediately stop using the recalled ski boots and contact SCARPA for instructions on returning the boot to receive a free boot shell repair. SCARPA is contacting all known purchasers directly.

Consumers may contact SCARPA toll-free at (866) 998-2895 from 8 a.m. to 5 p.m. (MT) Monday through Friday, by email at recall@scarpa.com, or online at www.scarpa.com and click on “Fall 2017 Maestrale RS and Maestrale Ski Boot Recall” at the top of the page for more information.

Mazda North American Operations is recalling 69,879 model year 2007-2012 CX-7, CX-9 and model year 2009-2012 Mazda6 vehicles.

The vehicles had their passenger front airbag inflators previously replaced under a prior recall using inflators of the same design.

The inflators may explode due to propellant degradation occurring after long-term exposure to high absolute humidity, temperature and temperature cycling.

An inflator explosion may result in sharp metal fragments striking the driver or other occupants resulting in serious injury or death.

What to do

Mazda will notify owners, and dealers will replace the front passenger air bag inflator with an alternate one free of charge.

The recall is expected to begin December 18, 2019.

Owners may contact Mazda customer service at (800) 222-5500, option 4. Mazda's number for this recall is 1317F.

Vitamin Cottage Natural Food Market of Lakewood, Colo., is recalling Natural Grocers brand organic soybeans.

The product may contain mold.

The following product, packaged in clear plastic bags weighing two pounds and bearing the “Natural Grocers” label and the packed-on dates 19-168 and 19-205, are being recalled:

The packed-on date can be found in the bottom left-hand corner of the label.

The recalled product was shipped to 154 Natural Grocers’ stores located in Arkansas, Arizona, Colorado, Iowa, Idaho, Kansas, Louisiana, Minnesota, Missouri, Montana, Nebraska, Nevada, New Mexico, North Dakota, Oklahoma, Oregon, Texas, Utah, Washington and Wyoming.

Specific locations of those stores may be found here. 

What to do

Customers who purchased the recalled product should discontinue use and discard or return it to the store for credit or refund.

Consumers with questions may contact the company at (303) 986-4600, ext. 80801, Monday through Friday 8:00 a.m. to 5:00 p.m. (MST).

Forest River is recalling 19 model year 2020 Surveyor trailers, model SVT33KFKDS.

A fuse with incorrect amperage was installed for the 12V refrigerator, potentially allowing the wiring to overheat.

If the wiring overheats, an electrical short can occur, increasing the risk of a fire.

What to do

Forest River has notified owners, and dealers will replace the incorrect fuse with one of the correct amperage free of charge.

The recall began November 7, 2019.

Owners may contact Forest River customer service at (260) 499-2100. Forest River's number for this recall is 37-1108.

Grace Digital of San Diego, Calif., is recalling about 88,000

ECOXGEAR EcoBoulder speakers.

The speaker’s battery can become overcharged and burst, posing an impact hazard.

ECOXGEAR has received five reports of speaker batteries bursting and fragmenting, including two incidents of property damage to the surrounding area. No injuries have been reported.

This recall involves the ECOXGEAR EcoBoulder Bluetooth Speakers., which is black in color with a rubber slip mat on top and about 20” tall and 15” wide.

There are four versions which have a color accent around the front speaker and a matching rubber slip mat. There is a storage compartment located on the left side of the speaker.

The model number GDI-EXBM900 series is labeled on the inside door of the speaker’s storage compartment.

ECOXGEAR is printed on the front of the speakers.

The speakers, manufactured in China, were sold at Costco stores nationwide from October 2016, to January 2017, at Academy Sports, Cabela’s, Home Depot and Best Buy stores nationwide and online at Amazon.com from January 2018, through December 2018, for about $180.

What to do

Consumers should immediately stop using the recalled speakers and contact ECOXGEAR to receive a free battery replacement kit.

Consumers may contact ECOXGEAR at (800) 903-9664 from 8 a.m. to 8 p.m. (CT) Monday through Friday, by email at safety@ecoxgear.com, or online at www.ecoxgear.com and click on "SAFETY ALERT" for EcoBoulder at the top of the page header or at www.ecoxgear.com/safetynotice for more information.

Keystone RV Company is recalling 157 model year 2019-2020 Crossroads Sunset trailers, model 242BH.

The interior range cooktop is installed in a cabinet that may not be entirely sealed from the furnace cavity. As a result, during furnace operation, the interior range cooktop burner flame may invert.

If the cooktop burner flames invert, there is an increased risk of a fire and injury.

What to do

Keystone will notify owners, and dealers will inspect the interior range cooktop with the furnace running, sealing it as necessary, free of charge.

The recall is expected to begin December 16, 2019.

Owners may contact Keystone customer service at (866) 425-4369. Keystone's number for this recall is 19-362.

Deck Source of Canada is recalling about 1,850 containers of Cutek Proclean Professional Wood Restoration sold in the U.S., and Canada.

The product contains the hazardous substance oxalic acid. The product label violates the Federal Hazardous Substance Act by omitting the word “poison” and printing the mandatory hazard statement for poisonous chemicals on the back of the label instead of the front, posing a risk of poisoning if swallowed by children.

No incidents or injuries are reported.

This recall involves Cutek Proclean Professional Wood Restoration, sold in a clear plastic one-gallon bottle with a blue, black and white label.

“Cutek Proclean Professional Wood Restoration” is printed on the front of the product and UPC 098411800166 is printed on the side panel of the product.

The wood restoration product, manufactured in Australia, was sold at DK Sales, Meteek Supply, Alpine Lumber, Thermory USA, Niece Lumber, Shipshe Sealers and Gable Lumber from May 2014, through October 2019, for about $65.

What to do

Consumers should immediately stop using the recalled product, move it out of the reach of children and contact Deck Source for a free replacement label to put on the product.

Consumers may contact Deck Source toll-free at (844) 442-8835 from 9 a.m. to 4 p.m. (ET) Monday through Friday, by email at sales@cutekstain.com or online at www.cutekstain.com and click on “Contact Us” at the top of the page for more information.

B&B Acquisition of Salt Lake City, Utah, is recalling about 67,700 packages of Airome Wintergreen Essential Oil and Deep Soothe Essential Oil 100 percent Pure & Natural Therapeutic Grade Essential Oils.

The product contains the substance methyl salicylate, which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA).

The packaging of the product is not child resistant, posing a poisoning risk if the contents are swallowed by young children.

No incidents or injuries are reported.

This recall involves Airome Wintergreen 100% pure essential oils in 0.5- and 0.34-fluid-ounce amber glass dropper bottles sold without a child-resistant cap.

It also includes Airome Deep Soothe 100% pure essential oils in 0.5-fluid-ounce amber glass dropper bottles sold without a child-resistant cap.

Each bottle has a black cap and blue label with either “Airome Wintergreen 100% Pure Essential Oil Stimulate” or “Airome Deep Soothe 100% Pure Essential Oil Cool” printed on the front. A UPC code unique to each type of recalled bottle –83324503131, 833245034567, or 833245035977 – is printed on the bottom of the gift box in which the bottles were sold.

The Arome Wintergreen 100% Pure Essential Oil Stimulate was sold separately and as part of a 3-pack “Focus & Concentrate Essential Oil Gift Set.”

The oils, manufactured in the U.S., were sold at home specialty stores and gift shops nationwide and online at Amazon.com from December 2016, through July 2019, for between $12 and $20.

What to do

Consumers should immediately store the product in a safe location out of the reach of children and contact B&B Acquisition for a free replacement child-resistant cap.

Consumers may contact B&B Acquisition at (800) 262-2305 from 8 a.m. to 5 p.m. (MT) Monday through Friday or by email at info@airome.com.

Mazda North American Operations is recalling 146 model year 2019 CX-9s equipped with Sumitomo Falken ZIEX CT50 A/S tires, size P255/50R20 104V -- date code 1619.

An incorrect rubber compound may have been used in the tire's manufacturing, allowing the tread to separate and detach.

A detached tire tread can decrease vehicle stability and increase the risk of a crash.

What to do

Mazda will notify owners, and dealers will inspect all four tire serial numbers, replacing the tires as necessary free of charge.

The recall is expected to begin December 18, 2019.

Owners may contact Mazda customer service at (800) 222-5500, Option 4. Mazda's number for this recall is 4019J.

United National Closeout Stores (UNCS) of Fort Lauderdale, Fla., is recalling about 1,500 ISO7X isometric exercise devices.

The handle grips on each end can break during use and cause parts to be ejected forcefully from the shaft, posing a risk of injury from impact to the user or bystander.

The firm has received 10 reports of the handles breaking and the ejection of the internal spring coil and rod, including five reports of impact injuries that resulted in punctures and lacerations.

This recall involves Ontel ISO7X isometric exercise devices.

The device is about three feet long with hard plastic black handle grips on each end and two black nylon straps that extend down opposite sides of the center metal shaft.

Only isometric exercise devices with black handle grips are involved.

The exercise devices, manufactured in China, were sold at Burlington Stores nationwide from January 2019, through March 2019, for about $7.

What to do

Consumers should immediately stop using the recalled device and contact UNCS to receive instructions on how to obtain a full refund.

Consumers may contact UNCS collect at (954) 524-3325 from 8 a.m. to 5 p.m. (ET) Monday through Friday or by email at email help@uncs.com.

Forest River is recalling 27 model year 2020 East to West Delta Terra (model 312BH) and East to West Silver Lake (model 31KBH) recreational trailers.

The overhead bunk fasteners may not be properly secured to the backer board of the bunk.

As a result, the bunk may fall, posing an injury risk.

What to do

Forest River has notified owners, and dealers will secure the bunk to the backer properly free of charge.

The recall began November 1, 2019.

Owners may contact Forest River customer service at (574) 264-6664. Forest River's number for this recall is 500-1112.

Kettle Cuisine of Lynn, Mass., is recalling Marketside Brand Creamy Cauliflower Parmesan Soup.

The product may contain fish and wheat, allergens not declared on the label.

No adverse reactions or illnesses have been reported to date.

The recalled product is packed into 16-oz plastic retail lidded cups labeled as ‘Marketside Brand Creamy Cauliflower Parmesan Soup’ with UPC 8113130636 and use-by dates ranging from 11/23/19 to 01/01/20 inclusive.

It was distributed to Walmart stores in all 50 states for purchase in store or online.

What to do

Customers who purchased the recalled product should dispose of it or return it to the store where purchased for a refund.

Consumers with may contact Kettle Cuisine at (617) 409-1290 between 9AM and 5PM EST, Monday through Friday.

Thor Motor Coach (TMC) is recalling 378 model year 2019-2020 Chateau 22B, 22E, 23U, 24F, 25V, & 28A, Daybreak 22GO, Four Winds 22B, 22E, 24F, 26B & 28A, Freedom Elite 22HE, and 2020 Quantum GR22 & SE22 motorhomes.

The seatbelt-unfastened warning light will not illuminate for approximately five seconds after the ignition is moved to the "on" or "start" position.

Without the seatbelt warning reminder, the driver may forget to fasten the seatbelt, increasing the risk of injury in a crash.

What to do

TMC owners will be notified, and dealers will reprogram the instrument panel cluster free of charge.

The recall began October 3, 2019.

Owners may contact Chevrolet customer service at (800) 630-2438, GMC customer service at (800) 462-8782 or TMC customer service at (877) 855-2867. TMC's number for this recall is RC000177.

Amneal Pharmaceuticals of Bridgewater, N.J., is recalling Ranitidine tablets and syrup.

The products are contaminated with N-Nitrosodimethylamine (NDMA), a probable human carcinogen, above levels established by the FDA.

The products are used for multiple indications, including treatment and prevention of ulcers of the stomach and intestines and treatment of gastroesophageal reflux disease.

There are no reports of adverse events.

Products with the following lot numbers are being recalled:

The Ranitidine tablets and syrup being recalled can be identified by the following NDC numbers, which are on the product label:

What to do

Patients who have experienced any problems that may be related to the use of this recalled product. should contact their physician or healthcare provider

Consumers who have the recalled products should stop using them and can call Stericycle at (866) 918-8768, Monday – Friday, 8:00 am – 5:00 pm (EST) for further information.