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. 2,467 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,467 in last 12 months

Showing 2778127800 of 50,591 recalls

Medical DeviceNovember 3, 2017· Volcano Corporation

Recalled Item: Volcano Imaging System s5i Recalled by Volcano Corporation Due to On certain...

The Issue: On certain Impacted Systems, an unexpected Microsoft Windows Security dialog...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Handicare Usa Inc

Recalled Item: Handicare P600 Series Patient Lift Product Usage: A device used Recalled by...

The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Handicare Usa Inc

Recalled Item: Handicare C Series Patient Lift Product Usage: A device used Recalled by...

The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden Classic 38 Sphere Daily Wear Soft contact Recalled by Alden Optical...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver Xstar Safety Slit Knife: (a) Recalled by Beaver-Visitec...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver EdgeAhead Safety Knife Recalled by Beaver-Visitec International...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: NovaKone Daily Wear Soft contact Recalled by Alden Optical Due to Contact...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP59 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP49 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver Optimum Safety Sideport Knife: (a) Straight 15o Recalled by...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP49 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP54 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver Safety Sideport Knife: (a) 1.0mm Recalled by Beaver-Visitec...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP54 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP59 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: ASTERA Multifocal Toric Daily Wear Soft contact Recalled by Alden Optical...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
DrugNovember 3, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: bupPROPion HCL Extended-Release Tablets Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Mylan Pharmaceuticals Inc. is...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 2, 2017· Remel Inc

Recalled Item: CM0405 Mueller-Hinton Broth IVD Recalled by Remel Inc Due to Product may...

The Issue: Product may have incorrect cation information detailed on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2017· Pro-Med Instruments Gmbh

Recalled Item: pmi Recalled by Pro-Med Instruments Gmbh Due to The firm received reports of...

The Issue: The firm received reports of two breakages of the pin tips which occurred...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2017· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: NeoBase Succinylacetone Assay Solution Recalled by PerkinElmer Life and...

The Issue: There is a potential for leaking vials for certain lot numbers where, if...

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

Class II — Potential Health HazardOngoing