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. 1,807 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
1,807 in last 12 months

Showing 3432134340 of 51,202 recalls

FoodMay 23, 2016· Let's Do Lunch, Inc.

Recalled Item: Integrated Food Service Turkey Bologna & Cheese Sandwich Turkey Bologna...

The Issue: Potential Listeria monocytogenes contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 23, 2016· Let's Do Lunch, Inc.

Recalled Item: Integrated Food Service Turkey Ham & Cheese Sandwich on a Recalled by Let's...

The Issue: Potential Listeria monocytogenes contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 23, 2016· Let's Do Lunch, Inc.

Recalled Item: Cafe Favorites Oven Roasted Turkey Breast Sub Code #C02284/02284 Recalled by...

The Issue: Potential Listeria monocytogenes contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 23, 2016· Let's Do Lunch, Inc.

Recalled Item: Integrated Food Service Submarine on a French Roll Turkey Bolo Recalled by...

The Issue: Potential Listeria monocytogenes contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 23, 2016· Let's Do Lunch, Inc.

Recalled Item: Integrated Food Service Chicken Patty Sandwich Chicken Patty on a Recalled...

The Issue: Potential Listeria monocytogenes contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· DeVilbiss Healthcare LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Ev3, Inc.

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.

Class II — Potential Health HazardOngoing
FoodMay 20, 2016· Ultimate Nutrition, Inc.

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.

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2016· Ultimate Nutrition, Inc.

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.

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2016· Ultimate Nutrition, Inc.

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.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 20, 2016· Merz North America, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2016· Integra LifeSciences Corp.

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.

Class II — Potential Health HazardOngoing
DrugMay 19, 2016· West-Ward Columbus Inc

Recalled Item: Oxycodone HCl Recalled by West-Ward Columbus Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specification; 9 month stability

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMay 19, 2016· Galderma Laboratories, L.P.

Recalled Item: Doxycycline Recalled by Galderma Laboratories, L.P. Due to Labeling:...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: Some expiries and lot...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund