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. 2,566 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,566 in last 12 months

Showing 1586115880 of 28,641 recalls

Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· DePuy Orthopaedics, Inc.

Recalled Item: CORAIL Cementless Femoral Stem HA Coated Standard Size 11 Recalled by DePuy...

The Issue: Two lots of femoral stems were labeled as Size 11. However, they are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...

The Issue: The flow rate test verification was not properly executed for certain Sigma...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Skull Pin Recalled by Ossur Americas Due to Halo system products...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur CB Resolve Recalled by Ossur Americas Due to Halo system products...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur OB Resolve Recalled by Ossur Americas Due to Halo system products...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Skull Pin Recalled by Ossur Americas Due to Halo system products...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2018· Espiner Medical Ltd

Recalled Item: Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml...

The Issue: Label was incorrect. The label states that the volume of the retrieval bag...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2018· Boston Scientific Corporation

Recalled Item: Boston Scientific Maestro 4000 Cardiac Ablation System Recalled by Boston...

The Issue: Reports of unintended continuation of radiofrequency (RF) energy delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2018· Nico Corp.

Recalled Item: NICO Shepherd' s Hook - Greenberg Recalled by Nico Corp. Due to Mislabeling

The Issue: Mislabeled hook pouch included a transport/storage label rather than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2018· Stryker Sustainability Solutions

Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...

The Issue: Through investigation, it was determined that H12LP Trocars in scope of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2018· Bovie Medical Corporation

Recalled Item: J-Plasma Precise 360 Recalled by Bovie Medical Corporation Due to There is a...

The Issue: There is a potential risk associated with the PEEK tip of the J-Plasma...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2018· Compass Health Brands (Corporate Office)

Recalled Item: CPAP Mask Cushion Recalled by Compass Health Brands (Corporate Office) Due...

The Issue: A May 2015 design change in the cushion seal replacement part and...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 18, 2018· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Oasis MRI system Product Usage: Hitachi MR system is Recalled by...

The Issue: The stainless steel belt which runs the length of the table underneath the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2018· Medline Industries Inc

Recalled Item: Endoscopic Cleaning Brush Recalled by Medline Industries Inc Due to There is...

The Issue: There is potential risk of brush detachment during cleaning. If brush...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2018· Maquet SAS

Recalled Item: VOLISTA StandOP Surgical Light Recalled by Maquet SAS Due to Certain VOLISTA...

The Issue: Certain VOLISTA StandOP Surgical Lights have been identified as having a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Beekley Corporation

Recalled Item: O-SPOT Recalled by Beekley Corporation Due to There is a potential for...

The Issue: There is a potential for imaging artifact to mimic calcifications on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Smith & Nephew, Inc.

Recalled Item: JOURNEY BCS OXINIUM Knee Femoral Components Recalled by Smith & Nephew, Inc....

The Issue: The data in the National Joint Registry of England, Wales and Northern...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Smith & Nephew, Inc.

Recalled Item: JOURNEY BCS Knee Conventional Polyethylene Inserts: 74023111 Recalled by...

The Issue: The data in the National Joint Registry of England, Wales and Northern...

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

Class II — Potential Health HazardOngoing