Product Recalls in Louisiana
Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,487 recalls have been distributed to Louisiana in the last 12 months.
Showing 34321–34340 of 51,202 recalls
Recalled Item: BACKROAD COUNTRY ROASTED AND SALTED SUNFLOWER SEEDS Recalled by Troyer...
The Issue: The product has been recalled because it has the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Yogurt Trail Mix under the following labels: 1) 15 LB Recalled by First...
The Issue: Product has the potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BACKROAD COUNTRY PEANUT BUTTER PRETZELS Recalled by Troyer Cheese Inc Due to...
The Issue: The product has been recalled because it has the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
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: 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: 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 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 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 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 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: DeVilbiss Model 7305P-D Powered Suction Unit Recalled by DeVilbiss...
The Issue: A small percentage of units of 7305 Series Vacu-Aide Suction Units are...
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 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: 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 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 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: Product is packaged into a plastic bag and placed into Recalled by Woodland...
The Issue: Sunflower seeds purchased from SunOpta that are potentially contaminated...
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.