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. 2,469 recalls have been distributed to Louisiana in the last 12 months.
Showing 37801–37820 of 51,202 recalls
Recalled Item: CARESTREAM DRX-EVOLUTION X-Ray System Product Usage: The device is a...
The Issue: Software defect that impacts image alignment when using the automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI 500 Blood Parameter Monitoring System. Provides continuous Recalled by...
The Issue: Inaccuracies in SvO2, temperature, pH, pCO2, pO2, Hematocrit, and Potassium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar" Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Triple Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due to...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR"* 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled by...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due to...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled by...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Saline Flush Prefill Double Pouch Item Code: 8881570129...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Triple Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temporary Total Artificial Heart (TAH-t) with Freedom Driver System by...
The Issue: SynCardia Systems, Inc. is recalling Freedom Drivers due to a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Combo Set Case The cases hold surgical instrumentation in Recalled by...
The Issue: The lids on implant caddies within P/N 17-5000 and 19-5000 could not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thinflap System Case The cases hold surgical instrumentation in place...
The Issue: The lids on implant caddies within P/N 17-5000 and 19-5000 could not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DuraPrep Surgical Solution Iodine Povacrylex (0.7% Available Iodine) and...
The Issue: Chemical contamination: Product may be contaminated with a toxic compound.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LiDa DAIDAIHUA (also packaged as LiDa DAIDAIHUAJIAONANG) Recalled by Blue...
The Issue: Marketed Without An Approved NDA/ANDA: presence of undeclared Sibutramine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.