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 2802128040 of 50,591 recalls

Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults with BALLARD Technology WET...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: NOVAPLUS* Endotracheal WET PAK* Closed Suction System for Adults with...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
DrugOctober 5, 2017· Purdue Pharma, LP

Recalled Item: Betadine Solution Swabstick Povidone-Iodine Solution USP Recalled by Purdue...

The Issue: Subpotent Drug: The laminate used to make the pouches was reversed such that...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 5, 2017· Monteris Medical Corp

Recalled Item: MONTERIS MEDICAL NEUROBLATE SYSTEM Recalled by Monteris Medical Corp Due to...

The Issue: The firm received complaints that involved an unanticipated interaction...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 5, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Network Firewall (Cisco ASA 5506) Recalled by Philips Electronics...

The Issue: Firewall installed with Philips IntelliVue Information Center iX or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2017· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: 2008T Recalled by Fresenius Medical Care Renal Therapies Group, LLC Due to...

The Issue: While reviewing documentation for the next software release of the 2008T, an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2017· Teleflex Medical

Recalled Item: WECK(R) from TELEFLEX Auto Endo5(R) Recalled by Teleflex Medical Due to The...

The Issue: The product has a non-conformity that may cause clips to mislead, jam or...

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

Class II — Potential Health HazardOngoing
DrugOctober 3, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Famotidine tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Famotodine has an out of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 3, 2017· Becton Dickinson & Co.

Recalled Item: Difco" Agar Noble Recalled by Becton Dickinson & Co. Due to Mislabeling

The Issue: HighPuragar was mislabeled and inadvertently sold as Noble Agar.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2017· Zimmer Biomet, Inc.

Recalled Item: Sirus Drill 13mm diameter trauma instrument used for preparation of Recalled...

The Issue: The Sirus Drill and Flexible Shaft instruments may not be adequately cleaned...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2017· Zimmer Biomet, Inc.

Recalled Item: Flexible Shaft hip and anatomical shoulder instrument used for preparation...

The Issue: The Sirus Drill and Flexible Shaft instruments may not be adequately cleaned...

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

Class II — Potential Health HazardOngoing
DrugOctober 2, 2017· Unichem Pharmaceuticals Usa Inc

Recalled Item: Bisoprolol Fumarate tablets Recalled by Unichem Pharmaceuticals Usa Inc Due...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification for an...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 2, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Go.Up computed tomography (CT) x-ray system table Recalled by...

The Issue: The table may become unstable if the nuts on the bolts were not adequately...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Go.Now computed tomography (CT) x-ray system table Recalled by...

The Issue: The table may become unstable if the nuts on the bolts were not adequately...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2017· Edwards Lifesciences, LLC

Recalled Item: Hemosphere System with the following three components: HEM1 Advanced Monitor...

The Issue: Pre-procedural issues related to software defects

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

Class II — Potential Health HazardOngoing