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 34381–34400 of 51,202 recalls
Recalled Item: white and dark chocolate peanut clusters Recalled by The Caramel Factory,...
The Issue: Candy, baked goods, and Caramel icing contain undeclared allergens....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: sugar free milk chocolate cashew cluster Recalled by The Caramel Factory,...
The Issue: Candy, baked goods, and Caramel icing contain undeclared allergens....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: chocolate covered Twinkies Recalled by The Caramel Factory, LLC. Due to...
The Issue: Candy, baked goods, and Caramel icing contain undeclared allergens....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: pecan fudge Recalled by The Caramel Factory, LLC. Due to Undeclared Allergens
The Issue: Candy, baked goods, and Caramel icing contain undeclared allergens....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pralines Recalled by The Caramel Factory, LLC. Due to Undeclared Allergens
The Issue: Candy, baked goods, and Caramel icing contain undeclared allergens....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: salt water taffy Recalled by The Caramel Factory, LLC. Due to Undeclared...
The Issue: Candy, baked goods, and Caramel icing contain undeclared allergens....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Proteus 235 and Proteus ONE proton therapy systems Recalled by Ion Beam...
The Issue: Recall is being initiated to address on-site software installations not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA Standard with Compressor ventilator Recalled by Carefusion 211 Inc dba...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gas Delivery Engine (GDE)- Recalled by Carefusion 211 Inc dba Carefusion Due...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas¿ Liat Influenza A/B Quality Control Kit Recalled by Roche Molecular...
The Issue: Kit labeled with the incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calix T PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...
The Issue: The trials and rasps used to prepare the surgical site for placement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA Standard ventilator Recalled by Carefusion 211 Inc dba Carefusion Due...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Homocysteine Flex Reagent Cartridge (HCYS) Recalled by CSL...
The Issue: Reagent lots # 15243MA and 15243MB shows a reduced stability once opened...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA GDE/UIM upgrade kit Recalled by Carefusion 211 Inc dba Carefusion Due...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA Comprehensive ventilator- Recalled by Carefusion 211 Inc dba Carefusion...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calix P PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...
The Issue: The trials and rasps used to prepare the surgical site for placement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dome Centric component ( 01.04227.005) from the Anatomical Shoulder (AS)...
The Issue: In some cases it has been difficult or not possible to disassemble the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TCA Board Recalled by Carefusion 211 Inc dba Carefusion Due to CareFusion...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA Comprehensive ventilator Recalled by Carefusion 211 Inc dba Carefusion...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calix P PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...
The Issue: The trials and rasps used to prepare the surgical site for placement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.