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. 2,678 recalls have been distributed to Louisiana in the last 12 months.
Showing 8941–8960 of 29,201 recalls
Recalled Item: Cardinal Health Poly-Reinforced Surgical Gowns XX-large SKU: 9070 Recalled...
The Issue: Potential for open packaging seals compromising the sterility of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartGown Breathable Surgical Gowns with raglan sleeves X-large Recalled by...
The Issue: Potential for open packaging seals compromising the sterility of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Poly-Reinforced Surgical Gowns X-large SKU: 9040 Recalled by...
The Issue: Potential for open packaging seals compromising the sterility of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RoyalSilk Non-Reinforced Surgical Gowns XXX-large Recalled by Cardinal...
The Issue: Potential for open packaging seals compromising the sterility of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Steripath Gen2 Blood Collection System Model Number/Description...
The Issue: Due to an uptick of complaints associated with premature needle retraction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hanger-Bar 2P 45cm Recalled by Human Care USA, Inc. Due to The Hanger-Bar is...
The Issue: The Hanger-Bar is being recalled due to the potential for the set screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hanger-Bar 2P 45cm Recalled by Human Care USA, Inc. Due to The Hanger-Bar is...
The Issue: The Hanger-Bar is being recalled due to the potential for the set screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&Nephew EVOS MEDIAL DISTAL FEMUR PLATE Recalled by Smith & Nephew, Inc....
The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE Recalled by Smith &...
The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE Recalled by Smith &...
The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew EVOS MEDIAL DISTAL FEMUR PLATE Recalled by Smith & Nephew, Inc....
The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol...
The Issue: When calibrating using the standard provided in the kit, the change in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diversatek Health Recalled by Diversatek Healthcare Due to M-Catch Retrieval...
The Issue: M-Catch Retrieval Nets, Part Number 1175-01 / Lot Number 001919, that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wireless Footswtich used with the following Philips Allura Xper and Recalled...
The Issue: Wireless foot switch connection issues causing interruption of Fluoroscopy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System:...
The Issue: The Instructions for Use have been updated to include: (1) Clarification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray...
The Issue: It was noticed in production on 28.10.2021, that the final testing database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 by...
The Issue: Due to consoles not in compliance with the latest electrical safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVLP Convenience Pack/Kit Recalled by Medline Industries Inc Due to NaCl 250...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous Access Pack-LF Convenience Kit Recalled by Medline Industries Inc Due...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Major Vascular CDS Convenience Kit Recalled by Medline Industries Inc Due to...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.