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. 2,509 recalls have been distributed to Alabama in the last 12 months.
Showing 18681–18700 of 28,641 recalls
Recalled Item: Covidien Kerlix Super Sponge Saline Dressing Recalled by Covidien LLC Due to...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The PreludeSYNC Radial Compression Device is a sterile Recalled by Merit...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Wet Dressing 8 x 4 (20.3 cm x 10.2 cm) Recalled by...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Eye Pad Oval Recalled by Covidien LLC Due to Product...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panta Nail Recalled by Integra LifeSciences Corp. Due to Voluntary...
The Issue: Voluntary recall/Removal of Panta and Panta XI Nails because there may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Eye Pad Item Code: 03201 The sterile eye Recalled by...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Saline Dressing 8' x 4 (20.3cm x10.2 cm) Recalled by...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: It is recommended for patients with weight/size between 4-22 lbs Recalled by...
The Issue: Product labeled as GVL 2 Stat (blades), lot GC32825, was physically packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.