2013 Product Recalls

5,512 recalls issued in 2013.

5,512
Total Recalls
290
CPSC
1,377
FDA Drug
1,026
FDA Device
CPSC 290 FDA Drug 1,377 FDA Device 1,026 NHTSA 708 FDA Food 2,111

Showing 5461–5480 of 5,512 recalls

CPSC

2013 Polaris Ranger® 400 recreational off-highway vehic Recalled for Crash Hazard

The recreational vehicle's throttle can fail to operate properly, which can cause the vehicle's rider to lose control, posing a crash hazard.

Consumers should immediately stop using the recalled Polaris Ranger vehicles and contact Polaris to schedule a free repair. Polaris is contacting its customers directly.
FDA Class I

La Madeleine Potato Soup, 5 lb clear Cryovac pouches, 4 pouches per case.

The potato in the potato soup is treated with sulfites. Sulfites were not declared on the firm's product label.
FDA Class II

Sanh Yuan Preserved Plum Candy (Sweet and Sour Prune), 5 oz (142g)

CHO Fuku Group Inc. is recalling Sanh Yuan Preserved Plum Candy (Sweet and Sour Prune) because of unacceptable levels of lead.
CPSC

Omni-Heat™ Lithium-Polymer Rechargeable Batteries Recalled for Fire Hazard

The batteries have a cell defect which can cause overheating, posing a fire hazard.

Consumers should immediately check the battery packs included with the electric jacket to determine if they are part of the recall. Those with affected batteries should immediately remove the affected battery pack(s) from the jacket and contact Columbia Sportswear for a free replacement.
FDA Class II

Nature's Plus GLUTEN Free SPIRU-TEIN HIGH PROTEIN ENERGY MEAL, S'mores (Flavor), 1.2 OZ. (34g) Packet, Display Box Product No. 95903, Individual Packet Product No. 45905, UPC Code 097467459052. There are 8 foil packets per corrugated display box. --- Serving Size - 1 packet (1.2 oz.).

One lot of 1.2 oz. packets of Spiru-tein High Protein Energy Meal, S'mores flavor, is labeled as "Gluten Free" but actually contains gluten. Lot 1243522 of the product with Best Buy Date 06 2016 is being recalled.
FDA Class II

Hemp Plus Granola. The product is packaged in a 25 lb. container. The UPC is 0 58449 88001 1. The product is labeled in parts: "***HempPlus Granola***INGREDIENTS: Organic rolled oats, organic evaporated cane juice, organic soybean oil, organic brown rice flour, organic flax seeds, organic hemp seed, organic oat syrup solids (organic oat syrups solids, tocopherol, sea salt, organic molasses***25 lb.***Nature's Path Foods, Blaine, WA 98230***www.naturespath.com***".

Undeclared almond. Vanilla Almond Granola which contains almonds but it was mis-labeled as Hemp Plus Granola and almond was not declared on label.
FDA Class I

Methylprednisolone Acetate (PF) 40 mg/ml Injection, supplied in 1 mL, 2 mL and 5 mL vials, manufactured by New England Compounding Center, Framingham, MA

Non-Sterility
FDA Class II

Glycerin 100% PF, 1mL, 2 mL, and 5 mL vials, manufactured by New England Compounding Center, Framingham, MA

Lack of Assurance of Sterility
FDA Class I

Methylprednisolone Acetate 40 mg/mL Injection, Preserved, supplied in 5 mL and 10 mL vials, manufactured by New England Compounding Center, Framingham, MA

Non-Sterility
FDA Class II

Isovue 200 mg/mL PF and 300 mg/mL PF, Vials, manufactured by New England Compounding Center, Framingham, MA

Lack of Assurance of Sterility
FDA Class II

Omnipaque 240mg/mL PF, 300mg/mL PF, in 3 mL, 5 mL, and 10 mL, vials, manufactured by New England Compounding Center, Framingham, MA

Lack of Assurance of Sterility
FDA Class II

Saline 10% and 3%, in 5 mL and 10 mL vials, manufactured by New England Compounding Center, Framingham, MA

Lack of Assurance of Sterility
FDA Class II

Triamcinolone 10 mg/mL P, 40mg/mL P, 40mg/mL PF and 80 mg/mL PF in 1 mL, 2 mL, 5 mL, and 10 mL vials, manufactured by New England Compounding Center, Framingham, MA

Lack of Assurance of Sterility
FDA Class II

Lidocaine 1% PF, 2% PF, and 4% PF, in 1 mL, 2 mL, 5 mL, and 10 mL vials, manufactured by New England Compounding Center, Framingham, MA

Lack of Assurance of Sterility
FDA Class II

Epinephrine Injection USP, 1 mL, USP 1:1000 (1 mg/mL), SQ/IM, Hospira, Inc., Lake Forest, IL --- NDC 0409-7241-01

Presence of Particulates; may contain glass particles
FDA Class II

Betamethasone Repository 6 mg/mL PF Injection and Betamethasone Repository 6 mg/mL P Injection, manufactured by New England Compounding Center, Framingham, MA

Lack of Assurance of Sterility
FDA Class II

Betamethasone Sodium Phosphate 6 mg/mL P Injection, Betamethasone Sodium Phosphate 6 mg/mL PF Injection, Betamethasone Sodium Phosphate 8 mg/mL PF Injection, Betamethasone Sodium Phosphate 12 mg/mL PF Injection, manufactured by New England Compounding Center, Framingham, MA

Lack of Assurance of Sterility
FDA