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 2794127960 of 50,591 recalls

Medical DeviceOctober 19, 2017· Cook Inc.

Recalled Item: Percutaneous Gastrojejunostomy Set Product Usage: Intended for the...

The Issue: Cook has identified that the affected lots may contain wire guides that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR Recalled by Johnson &...

The Issue: Some contact lenses were associated with complaints of a foreign matter...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: Small Patient ECC Pack BEQ-TOP 22301 Recalled by Datascope Corporation Due...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 49101 Childrens Large ECC Pack Recalled by Datascope Corporation Due...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS Recalled by Johnson &...

The Issue: Some contact lenses were associated with complaints of a foreign matter...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Cook Inc.

Recalled Item: Wills-Oglesby Percutaneous Gastrostomy Set Product Usage: Intended for the...

The Issue: Cook has identified that the affected lots may contain wire guides that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 5210 ECC Set - Respiratory Recalled by Datascope Corporation Due to...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BO-TOP 20700 SMALL PATIENT 3/8 Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: ECC Small - Respiratory BEQ-TOP 5210 Recalled by Datascope Corporation Due...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BO-TOP 13901 RAPID RESPONSE Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: Adult ECC Pack BEQ-TOP 22300 Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 33700 ECC 3/8" PACK Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 22301 Recalled by Datascope Corporation Due to The Better Bladder...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 27610 ECC PACK 3/8 Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 38900 ECC PACK Recalled by Datascope Corporation Due to The Better...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 22300 Recalled by Datascope Corporation Due to The Better Bladder...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 22702 ECC W/HMOD 30000 Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Cook Inc.

Recalled Item: Mallinckrodt Institute Percutaneous Gastrostomy Set Product Usage: Intended...

The Issue: Cook has identified that the affected lots may contain wire guides that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-T 25502 1/4 Better Bladder Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 8504 1/4X1/4 PACK W/QP Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing