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. 2,508 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,508 in last 12 months

Showing 2258122600 of 50,591 recalls

DrugApril 22, 2019· Inopak Ltd

Recalled Item: AQUACIL instant foaming hand sanitizer Recalled by Inopak Ltd Due to CGMP...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: ANTIBACTERIAL Foaming Hand Wash With Moisturizers labeled as Antibacterial...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: Sani-Guard-SF Waterless Foam Hand Sanitizer Recalled by Inopak Ltd Due to...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: Instant Waterless Hand Sanitizer Recalled by Inopak Ltd Due to CGMP...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: Mild Health Care Antibacterial Hand Soap Recalled by Inopak Ltd Due to CGMP...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: Antibacterial Hand Soap Recalled by Inopak Ltd Due to CGMP Deviations: hand...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: INODERM Antiseptic Hand Soap (E-2) Recalled by Inopak Ltd Due to CGMP...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: Antibacterial Hand Soap Recalled by Inopak Ltd Due to CGMP Deviations: hand...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: Unison Hand Care Products Recalled by Inopak Ltd Due to CGMP Deviations:...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: Carvedilol Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to Presence...

The Issue: Presence of Foreign Tablets/Capsules: Customer complaint for a small, solid,...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 22, 2019· Cook Inc.

Recalled Item: Cook Salle Intraoperative Pyeloplasty Stent Set PRODUCT/CATALOG NUMBER/GPN:...

The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2019· Cook Inc.

Recalled Item: Cook Kwart Retro-Inject Ureteral Stent Set: PRODUCT/CATALOG NUMBER/GPN: 4.7...

The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS4 Government Bundle Recalled by Philips North America, LLC Due...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS4 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips Healthcare Informatics, Inc.

Recalled Item: IntelliSpace PACS 4.4 Recalled by Philips Healthcare Informatics, Inc. Due...

The Issue: Images may potentially become corrupt while using the system.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Ethicon, Inc.

Recalled Item: ETHIBOND EXCEL¿ Polyester Suture-ETHIBOND Green 75cm USP1 Single Armed CT-1...

The Issue: Possibility that a suture raw material containing high endotoxin levels was...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing