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. 2,483 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,483 in last 12 months

Showing 2228122300 of 28,641 recalls

Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Stripper Recalled by American Medical Systems Innovation Center - Silicon...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Fiber Cleaver Recalled by American Medical Systems Innovation Center -...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Sureflex 910 Lithotripsy Fiber Recalled by American Medical Systems...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2015· Bard Access Systems

Recalled Item: PowerPICC SOLO Catheter with Sherlock 3CG TPS Stylet 4F Maximal Recalled by...

The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 27, 2015· Integra LifeSciences Corp.

Recalled Item: Integra Camino Intracranial Pressure Monitoring Catheter with Licox IMC Bolt...

The Issue: Integra LifeSciences is recalling the Camino Intracranial Pressure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2015· Bard Access Systems

Recalled Item: PowerPICC SOLO Catheter with Tip Location System (TLS) Stylet 4F Recalled by...

The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 27, 2015· Bard Access Systems

Recalled Item: PowerPICC SOLO Catheter with Sherlock 3CG (TPS) Stylet 5F Maximal Recalled...

The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 27, 2015· Bard Access Systems

Recalled Item: PowerPICC SOLO2 Catheter 4F Maximal Barrier Tray with Microintroducer...

The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 27, 2015· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: Allofix Insertion Kit Recalled by Musculoskeletal Transplant Foundation,...

The Issue: Musculoskeletal Transplant Foundation is recalling a certain lot of Allofix...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2015· Synthes, Inc.

Recalled Item: DePuy Synthes 6.5 mm Titanium Recon Screws w/T25 Stardrive (70mm Recalled by...

The Issue: certain lots of the Titanium Recon Screws (6.5mm ) were found to contain the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2015· Bausch & Lomb Surgical, Inc.

Recalled Item: Bausch & Lomb SoFlex SE Foldable intraocular Lens Product Usage: Recalled by...

The Issue: Haptics breaking during lens loading and insertion.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2015· Bausch & Lomb Surgical, Inc.

Recalled Item: Bausch & Lomb SofPort Advanced Optics Aspheric Lens Recalled by Bausch &...

The Issue: Haptics breaking during lens loading and insertion.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing