Product Recalls in Alabama
Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,442 recalls have been distributed to Alabama in the last 12 months.
Showing 37361–37380 of 50,591 recalls
Recalled Item: Maryland Dissector Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Driver Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curved Needle Driver Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maryland Bipolar Forceps Recalled by Intuitive Surgical, Inc. Due to In...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
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: 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: IBC Vascular Loop Catalog Number CH111 Recalled by International Biophysics...
The Issue: It was discovered that the heat seal placed onto sterile pouches may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBC Suction Wand Catalog Number 1990S Product Usage: The IBC Recalled by...
The Issue: It was discovered that the heat seal placed onto sterile pouches may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBC Aortic Punch Catalog Numbers APM40 Recalled by International Biophysics...
The Issue: It was discovered that the heat seal placed onto sterile pouches may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KABOOM action strips Recalled by Blue Square Market, Inc. Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: presence of undeclared Sulfoaildenafil.
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.
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: Caribou Chocolate Chip Toffee Pecan Biscotti Recalled by Caribou Coffee...
The Issue: Biscotti Almond and Biscotti Chocolate Chip Toffee Pecan are being recalled...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Caribou Almond Biscotti Recalled by Caribou Coffee Company Inc. Due to...
The Issue: Biscotti Almond and Biscotti Chocolate Chip Toffee Pecan are being recalled...
Recommended Action: Do not consume. Return to store for a refund or discard.
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: 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: 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 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.