Product Recalls in Nebraska
Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,428 recalls have been distributed to Nebraska in the last 12 months.
Showing 33061–33080 of 49,150 recalls
Recalled Item: Integrated Food Service BBQ Rib Sandwich BBQ Rib Beef Patty Recalled by...
The Issue: Potential Listeria monocytogenes contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cafe Favorites 5" Super Sub on a Whole Grain Hoagie-IW Code #C02384/02384...
The Issue: Potential Listeria monocytogenes contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Integrated Food Service Chili Cheese Dog on Whole Grain Buns Code #809022...
The Issue: Potential Listeria monocytogenes contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Integrated Food Service Original Wienerschnitzel Chili Cheese Dog All Meat...
The Issue: Potential Listeria monocytogenes contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nitrofurantoin Oral Suspension Recalled by Nostrum Laboratories, Inc. Due to...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lodrane D (Brompheniramine maleate 4 mg and Pseudoephedrine HCl 60 mg)...
The Issue: Labeling: Not Elsewhere Classified: correctly labeled bottles were packaged...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TI Single Vector Distractor Body with Right Foot/30mm Recalled by Synthes...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Body with Left Foot/20mm Recalled by Synthes...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Proximal Foot/Left Recalled by Synthes (USA)...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Body with Right Foot/20mm Recalled by Synthes...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Body with Left Foot/30mm Recalled by Synthes...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrismaSate BGK2/0 Dialysis Solution for Continuous Renal Replacement Therapy...
The Issue: Presence of leaks near top of the PrismaSate bags
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EV3 EverFiex" Self-expanding Peripheral Stent System Recalled by Ev3, Inc....
The Issue: Medtronic is issuing a medical device recall to return product potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Proximal Foot/Right Recalled by Synthes (USA)...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiesse (+) Lidocaine Recalled by Merz North America, Inc. Due to...
The Issue: Complaints reported of Radiesse (+) unable to be expelled from the syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-wire Recalled by Integra LifeSciences Corp. Due to The affected K-wires do...
The Issue: The affected K-wires do not meet specification requirements. Specifically,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMATE NUTRITION AMINO GOLD CAPSULES SUPER WHEY FORMULA Dietary Supplement...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kroger SALTED SUNFLOWER KERNELS 6 oz (170g) INGREDIENTS: SUNFLOWER KERNELS...
The Issue: The firm was notified by their supplier that they are expanding their recall...
Recommended Action: Do not consume. Return to store for a refund or discard.