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. 2,700 recalls have been distributed to Louisiana in the last 12 months.
Showing 3581–3600 of 29,201 recalls
Recalled Item: Heparin Recalled by W L Gore & Associates, Inc. Due to Due to packaging...
The Issue: Due to packaging defects, sterility assurance and heparin activity may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...
The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Recalled by W L Gore & Associates, Inc. Due to Due to packaging...
The Issue: Due to packaging defects, sterility assurance and heparin activity may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobra Recalled by Neurovision Medical Products Inc Due to Mislabeling
The Issue: mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...
The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...
The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter PST 500 U Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX450 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX400 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX500 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX550 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Semi-rigid suction liners labeled as follows: a) SEMI RIGID Recalled...
The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventana anti-CD10 (SP67) Rabbit Monoclonal Primary Antibody Recalled by...
The Issue: Their is a potential for high background and off-target staining when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.