Recalls in November 2019

Forest River is recalling six model year 2020 Sunseeker SSC2250SLEC, Freelander FLC26RSC, and Leprechaun LPC240FSC vehicles.

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

Forest River will notify owners, and GM dealers will reprogram the instrument panel, free of charge.

The recall began on October 29, 2019.

Owners may contact GMC customer service at (800) 462-8782 or Forest River customer service at (800) 348-7440. Forest River's number for this recall is 51-1084.

Skacel Collection of Seattle, Wash., is recalling about 270 US 6 (4.0mm) addi FlipStix knitting needles.

The shaft of the knitting needle can split or burst, posing a laceration hazard.

The firm has received three reports of the needle shafts splitting. No injuries have been reported.

This recall involves US 6 (4.0mm diameter) FlipStix in 6” and 8” long knitting needles.

The knitting needles have aluminum shafts that are tapered at both ends. The long shaft holds the active (unsecured) stitches of the fabric, to prevent them from unravelling, whereas the tapered ends are used to form new stitches. The knitting needles were sold in blue, red and yellow combination packages, with five needles per pack.

The needles, manufactured in Germany, were sold at independent yarn stores nationwide from November 2018, through August 2019, for about $20.

What to do

Consumers should immediately stop using the recalled knitting needles and contact the store where purchased for a full refund in the form of a store voucher.

Consumers may contact Skacel Collection at (800) 255-1278 from 8 a.m. to 3:30 p.m. (PT) Monday through Friday, by email at recall@skacelknitting.com or online at www.skacelknitting.com/FlipStix_US6_Recall_Info for more information.

Mann Packing Co., is recalling a series of vegetable products sold to select retailers in the U.S. and Canada.

The products may be contaminated with Listeria monocytogenes.

There are no reported illnesses to date.

Lists of the recalled products, with “Best If Enjoyed By” dates of October 11, 2019, to November 16, 2019, are available here and here.

What to do

Customers who purchased the recalled products should discard them.

Consumers with questions may call customer service 24/7 at (844) 927-0707 or by email at consumers@mannpacking.com.

Ducati North America is recalling 793 model year 2019-2020 Hypermotard 950 and 950 SP motorcycles.

The negative terminal on the battery may break, potentially causing a sudden loss of power and an engine stall, which can increase the risk of a crash.

What to do

Ducati will notify owners, and dealers will inspect the routing of the negative cable, rerouting it as necessary. In addition, the battery will be better secured with insulation pads. These repairs will be performed free of charge.

The recall is expected to begin December 12, 2019.

Owners may contact Ducati customer service at (888) 391-5446. Ducati's number for this recall is SRV-RCL-19-003.

Nestlé USA is recalling various ready-to-bake refrigerated Nestlé Toll House Cookie Dough products.

The products may be contaminated with foreign material -- specifically food-grade rubber pieces.

No illnesses or injuries requiring medical treatment have been reported.

The following products, with batch codes that begin with 9189 through 9295, are being recalled:

The recalled products, sold in the continental U.S. and Puerto Rico, were assigned the following batch codes:

What to do

Customers who purchased the recalled products should not prepare or consume but discard them, and retain their proof of purchase and contact Nestlé Consumer Services at nestleproductinquiry@casupport.com.

Consumers with questions may contact the company 24/7 at (800) 681-1676 or by email at nestleproductinquiry@casupport.com.

Porsche Cars North America is recalling 44,128 of the following vehicles, superseding an earlier recall:

• Model year 2017 Panamera 4, Panamera Turbo & Panamera Turbo Executive
• Model year 2017-2018 Panamera, Panamera 4S Executive & Panamera 4S
• Model year 2018 Panamera Turbo S Hybrid, Panamera 4 Hybrid Sport Turismo, Panamera 4 Sport Turismo, Panamera Turbo S Hybrid Sport Turismo, Panamera 4 Hybrid & Panamera 4 Executive,
• Model year 2019 Cayenne Hybrid
• Model year 2019-2020 Cayenne, Cayenne S & Cayenne Turbo, and
• Model year 2020 Cayenne Coupe, Cayenne Turbo Coupe, & Cayenne S Coupe

The instrument cluster may not provide a visual warning when the brake pads are worn out.

If the driver is not alerted when brake pads are worn out, the vehicle may not respond as expected when braking, increasing the risk of crash.

What to do

Porsche will notify owners, and dealers will reprogram the instrument cluster free of charge.

The recall is expected to begin December 15, 2019.

Owners may contact Porsche customer service at (800) 767-7243. Porsche's number for this recall is AKB8.

Wawona Frozen Foods is recalling packages of frozen raspberries and frozen berry mixes containing raspberries.

The products may be contaminated with Hepatitis A.

No illnesses have been reported to date.

The following products, imported from Chile and sold at Adi and Raley stores, are being recalled:

• Season's Choice Raspberries (frozen): 12 ounce bags, "best by" date of June, 10, 2021, August 1,2021 and August 23, 2021. "Product of Chile." UPC Code: 0 41498 12419 9
• Season's Choice Berry Medley (frozen) containing raspberries: 16 ounce bags, "best by" date of July 17, 2021, July 20, 2021 and July 22, 2021. "Product of USA, Chile." UPC Code: 0 41498 31344 9
• Raley's Fresh Frozen Red Raspberries: 12 ounce bags, "best by" date of June 5, 2021 (lot code:20156A04), August 1, 2021 (lot code: 20213A06) "Product of Chile." UPC Code: 46567 00754

What to do

Customers who purchased the recalled products should not consume them, but discard or return them to the place of purchase for a full refund.

Consumers with questions may contact Wawona Frozen Foods at (866) 913-0667 or online at www.wawona.com.

Polaris is recalling 31,987 model year 2015-2019 Slingshot motorcycles.

Excessive electrical current may damage the battery fuse holder terminals.

Damaged terminals may result in the loss of forward and rear lighting, instrument cluster gauges or power steering assist, any of which could increase the risk of a crash.

What to do

Polaris will notify owners, and dealers will inspect the battery fuse block terminals and relocate the 50 amp chassis fuse free of charge.

The recall was expected to begin in October 2019.

Owners may contact Polaris customer service at (855) 863-2284. Polaris's number for this recall is T-19-01.

H&T Seafood of Bell, Calif., is recalling an undetermined amount of Siluriformes products (Swai filets).

The products, imported from Vietnam, were packed and distributed without undergoing USDA inspection, and used the mark of inspection without authorization.

There are no confirmed reports of adverse reactions.

The following frozen item, produced over an undetermined amount of time, is being recalled:

• 1-lb. plastic bags containing frozen fillets of “FISHERMAN’S WHARF SWAI FILLETS PRODUCT OF VIETNAM” with any USDA mark of inspection.

The recalled product was shipped to warehouse/distribution centers and retail locations in Florida, Georgia, Louisiana and South Carolina.

What to do

Customers who purchased the recalled product should not consume it, but discard or return it to the place of purchase.

Consumers with questions may contact Dat Huynh at (626) 679-1776.

Lannett Company is recalling all lots of Ranitidine Syrup.

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

The recalled product is used as a short-term treatment for active duodenal ulcers, maintenance therapy for duodenal ulcer patients, treatment of pathological hypersecretory conditions, short-term treatment of active, benign gastric ulcers, maintenance therapy for gastric ulcers, treatment of GERD and treatment of endoscopically diagnosed erosive esophagitis.

The following lots of the product, packaged in bottles of 16 fluid ounces (one pint) (NDC 54838-550-80), are being recalled:

The recalled product was distributed nationwide to wholesalers/distributors.

What to do

Patients should contact their physician or healthcare provider if they have any problems that may be related to taking or using the recalled product.

Deere & Company of Moline, Ill., is recalling about 8,500 John Deere 4044R, 4052R and 4066R compact utility tractors sold in the U.S., and Canada.

Front cab support bolts that were torqued improperly during manufacturing can fail during a rollover, posing a crushing injury hazard to the operator.

No incidents or injuries are reported.

This recall involves green and yellow compact utility tractors with “John Deere” and the model numbers 4044R, 4052R or 4066R printed on the hood.

Each of the recalled compact utility tractors has a 17-digit serial number located on the right side of the frame above the front axle.

Each serial number included in the recall begins with “1LV” and ends with a six-digit number that falls within the ranges below:

Model             Serial Number Range

4044R             400284 - 401619

4052R             400381 – 403424

4066R             401588 - 407220

The tractors, manufactured in the U.S., were sold at John Deere dealers nationwide from October 2016, through September 2019, for between $40,000 and $50,000.

What to do

Consumers should immediately stop using the recalled compact utility tractors and contact an authorized John Deere dealer for a free repair. John Deere is contacting all known purchasers directly.

Consumers may contact Deere & Company at (800) 537-8233 from 8 a.m. to 6 p.m. (ET) Monday through Friday, and 9 a.m. to 3 p.m. (ET) on Saturday, or online at www.deere.com and click on “Recalls” on the drop-down menu under “Parts & Services” at the top of the page for more information.

Golden Dragon Fortune Cookies of Chicago, Ill., is recalling Golden Dragon Chinese Almond Cookies.

The product may contain milk, an allergen not declared on the label.

No illnesses have been reported to date.

The recalled product is packaged in 5-lbs. boxes that contain five, 100-count plastic bags of the Almond Cookies. It may have been purchased by consumers in either the 5-lbs. box or the 100-count plastic bags. Both have UPC code 0 80005 23031 2 and Best if Used Before 3/20.

The cookies were sold by retail stores and wholesalers in Chicago, Ill.

What to do

Customers who purchased the recalled product should return it to the place of purchase for a full refund.

Consumers with questions may contact the company at (312) 842-8199 Monday through Friday, 8AM to 5PM.

North Bay Produce of Traverse City, Mich., is recalling 2,297 cases and two bulk bins of fresh apples.

The products may be contaminated with Listeria monocytogenes.

No illnesses have been linked by health officials to this recall.

Recalled varieties include McIntosh, Honeycrisp, Jonathan, Fuji, Jonamac and Red Delicious apples sold in plastic bags under the Great Lakes, North Bay Produce Pure Michigan brands, as well as unbranded in clear plastic tote bags, white paper tote bags, and individually from retailers display trays.

The recalled products were shipped between October 16 – 21, 2019, from one North Bay facility to wholesalers, retailers and brokers in Florida, Illinois, Kentucky, Louisiana, Michigan, North Carolina, Texas and Wisconsin.

The following products are being recalled:

Apples purchased at retail prior to October 16th are not affected.

What to do

Customers who purchased the recalled products should not consume them, but discard or return them to the place of purchase.

Consumers with questions may contact the company at (231-929-4001, Monday-- Friday, 8am -- 5pm (ET) or online at www.northbayproduce.com.

Forest River is recalling 44 model year 2020 Shasta Oasis SST30QB and SST31OK trailers.

The trailers may have been built with an incorrect length axle hanger, allowing the axle to contact the chassis while the trailer is moving.

The axle hanger contacting the chassis can cause loss of vehicle control, increasing the risk of a crash.

What to do

Forest River will notify owners, and dealers will replace the equalizers free of charge.

The recall is expected to begin November 25, 2019.

Owners may contact Forest River customer service at (574) 528-8717. Forest River's number for this recall is 53-1100.

Novitium Pharma is recalling all quantities and lots of Ranitidine Hydrochloride capsules in the U.S.

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

The recalled product is used for treatment of duodenal ulcer, benign gastric ulcer, reflux esophagitis, post-operative peptic ulcer, Zollinger-Ellison Syndrome, and other conditions where reduction of gastric secretion and acid output is desirable.

The following products are being recalled: 

What to do

Patients should continue taking their medication and speak to their physician or pharmacist about alternate healthcare treatment options. Customers desiring to return product should contact the pharmacy from which it was purchased.

Consumers with questions may contact the company at (609) 469-5920 or by email at info@novitiumpharma.com.