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. 1,018 recalls have been distributed to Louisiana in the last 12 months.
Showing 23721–23740 of 51,202 recalls
Recalled Item: RUSCH CARE Premium Drain bag Recalled by Teleflex Medical Due to The device...
The Issue: The device labels are not UDI compliant. The missing UDI compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Urinary Drainage bag Recalled by Teleflex Medical Due to The device...
The Issue: The device labels are not UDI compliant. The missing UDI compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrex Burr Recalled by Arthrex, Inc. Due to Devices may generate excessive...
The Issue: Devices may generate excessive heat during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethyl Alcohol Enzymatic Assay Recalled by Lin-Zhi International Inc Due to...
The Issue: Shelf life of the product may be reduced due to degradation of the assay.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: aap Implante AG Recalled by AAP Implantate Ag Due to There is the potential...
The Issue: There is the potential for the Lambotte chisel to break at the welded piece...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 21Y14=S PushValve upper part Product Usage: The PushValves/ MagValves is...
The Issue: Some of the installed valve-inserts have a diameter smaller than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 21Y14 PushValve Product Usage: The PushValves/ MagValves is intended...
The Issue: Some of the installed valve-inserts have a diameter smaller than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 21Y15 MagValve Product Usage: The PushValves/ MagValves is intended...
The Issue: Some of the installed valve-inserts have a diameter smaller than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoDELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...
The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...
The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoDELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...
The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOLIS Microplate System (Catalog no. 89700) with TimeLiner Data Management...
The Issue: User-induced circumstances can contribute to the EVOLIS Microplate Processor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipoic Acid Injection (aka Alpha Lipoic Acid or Thioctic Acid) Recalled by...
The Issue: Presence of Particulate Matter: filmy/cloudy particulate observed in vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets Recalled by MAJOR PHARMACEUTICALS Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Insufflation tubing to be used with varies insufflator units. Recalled by...
The Issue: The sterile single-use tubing may contain higher ethylene oxide (EO)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC70 w/trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC30 w/ trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC70 Recalled by Philips North America, LLC Due to Philips...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC30 w/o trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nelaton Urinary Catheter Recalled by ConvaTec, Inc Due to An internal...
The Issue: An internal assessment of packaging confirmed the potential for a breach in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.