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. 2,033 recalls have been distributed to Louisiana in the last 12 months.
Showing 6021–6040 of 29,201 recalls
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: An unexpected shutdown of the IABP may occur due to failures of tantalum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Troponin I ES Calibrators Recalled by...
The Issue: Reagent packs could potentially contain incorrect wells, which will generate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: IABP may lose the ability to charge batteries in one or both bay slots....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Cytosponge Cell Collection Device Recalled by Covidien, LLC Due to...
The Issue: Cell Collection Device may be at increased risk of the sponge detaching from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Reusable Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM Crea Test Card with epoc Host SW v3.37.3 Recalled by Siemens...
The Issue: There is potential for discrepant high glucose results in samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM Test Card (BUN & TCO2) Recalled by Siemens Healthcare Diagnostics...
The Issue: There is potential for discrepant high glucose results in samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM BUN Test Card with epoc Host SW v3.37.3 Recalled by Siemens...
The Issue: There is potential for discrepant high glucose results in samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UFSK Treatment chair 500 XLE- Treatment chair for positioning and Recalled...
The Issue: Service life of the electrical seat part drive of the treatment chair may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Osteomed, LLC Due to Screws for osteotomies have contain an...
The Issue: Screws for osteotomies have contain an undersize screwhead which has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trexo Device Recalled by Trexo Robotics Holdings Inc. Due to Electrical...
The Issue: Electrical issues that could potentially render the device non-functional,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Haemophilus Test Medium (Agar) (150mm) Recalled by Remel, Inc Due to...
The Issue: The test medium may not perform as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Osteomed, LLC Due to Screws for osteotomies have contain an...
The Issue: Screws for osteotomies have contain an undersize screwhead which has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.