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. 2,576 recalls have been distributed to Alabama in the last 12 months.
Showing 17301–17320 of 50,591 recalls
Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets 30 mg Recalled by...
The Issue: Failed Dissolution Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All EPIQ and Affiniti Ultrasound systems. Model numbers - EPIQ 5G Recalled...
The Issue: The manufacturer has determined that with certain uncommon workflows there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAC VU360 Recalled by GE Healthcare, LLC Due to Incorrect patient...
The Issue: Incorrect patient identification and/or patient demographic errors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MANI Infusion Cannula 23G S - Product Usage: for use Recalled by Mani, Inc....
The Issue: Dimensions of the Luer connector parts out of specification, may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MANI TROCAR KIT 23G S - Product Usage: for use Recalled by Mani, Inc. -...
The Issue: Dimensions of the Luer connector parts out of specification, may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Ascent...
The Issue: Presence of Foreign Tablet/Capsule: One bottle of Hydrocodone Bitartrate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Orally Disintegrating Tablets Recalled by Jubilant Cadista...
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer - Product Usage: automated Recalled by Siemens...
The Issue: Test Definition scanning may reset custom settings to defaults causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer - Product Usage: automated Recalled by Siemens...
The Issue: Test Definition scanning may reset custom settings to defaults. When a 2D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Felodipine Extended Release Tablets Recalled by Heritage Pharmaceuticals Inc...
The Issue: Failed impurities/ degradation specifications: Out of specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Nostrum...
The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Nostrum...
The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viral Transport Medium Recalled by Hardy Diagnostics Due to There is a...
The Issue: There is a potential for contamination within Viral Transport Media. Use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolut (TM) PRO System. With the following model numbers: a. EVOLUTPRO-23...
The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolut (TM) PRO+ System. With the following model numbers: a. Recalled by...
The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolut (TM) R System. With the following model numbers: a. EVOLUTR-23...
The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Biomeme SARS-CoV-2 Real-Time RT-PCR Test is a molecular in Recalled by...
The Issue: The firm has become aware of nine reports by a single customer that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Ultra-Fine Pen Needles 32G x 4mm (5/32' )-intended for Recalled by Becton...
The Issue: Product shelf cartons incorrectly labeled as products intended for the Latin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Box Label: ION Fully Articulating Catheter Recalled by Intuitive Surgical,...
The Issue: The distal tip ring of the fully articulating catheter may become dislodged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Pump - Product Usage: indicated for male patients suffering Recalled...
The Issue: Potential increased occurrence of pump fracture over the lifetime of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.