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 16361–16380 of 50,591 recalls
Recalled Item: RayCare 3B (3.1.0.60341) - Product Usage: Intended Use Oncology information...
The Issue: Patient related messages created in RayCare 3B, RayCare 4A will be lost when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software versions syngo.CT VA30A_SP2 or syngo.CT VA30A_SP2a in the Computed...
The Issue: SOMATOM systems-issues in with software syngo.CT VA30A_SP2 or syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acetaminophen Recalled by A-S Medication Solutions LLC. Due to Labeling:...
The Issue: Labeling: Label Mix-up; The bottle of over-the-counter Acetaminophen 500mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Menopur 75 IU Recalled by Ferring Pharmaceuticals Inc Due to Failed pH...
The Issue: Failed pH specifications: Out of Specification pH results for 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wilton Rainbow Chip Crunch Sprinkles Recalled by Wilton Industries Inc Due...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wilton Rainbow Chip Crunch Sprinkles Recalled by Wilton Industries Inc Due...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wilton Valentine Chip Crunch Sprinkles Recalled by Wilton Industries Inc Due...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wilton Autumn Assorted Treat Toppings Sprinkles Recalled by Wilton...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Holiday Home Assorted Treat Toppings Recalled by Wilton Industries Inc Due...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wilton Holiday Mix Sprinkles Recalled by Wilton Industries Inc Due to...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BCS XP System: Multipurpose system for in vitro coagulation studies....
The Issue: Siemens Healthcare Diagnostics Products GmbH has confirmed that the BCS XP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Assure COVID-19 IgG/IgM Rapid Test Device that include: 1) Pouch Recalled by...
The Issue: Due to Products being incorrect labeling "for diagnostic use" and labelled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Consist of a distal connection mechanism (either standard Terumo Ball...
The Issue: There is a potential for the stainless steel locking plates on the device's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Radiological Image Processing System - Product Usage:...
The Issue: The wrong patient information may be displayed in the viewer or PowerJacket.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automated Impella Controller (AIC) Recalled by Abiomed, Inc. Due to...
The Issue: Retrospective reporting for the release of Technical Bulletin IMP-2643 AIC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cellex qSARS-Cov-2 Antigen Rapid Test Recalled by Cellex Due to The kit does...
The Issue: The kit does not have an emergency use authorization (EUA).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyWay Walker Chassis - Product Usage: is intended for use Recalled by James...
The Issue: Due to a failure of the welds, the casters detached from the rear legs of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasonic pulsed doppler imaging system - Product Usage: intended for...
The Issue: Arietta 850 software version 4.0.0., 4.0.1, and 4.0.2 has an error in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Film 2mg/0.5mg Recalled by Alvogen,...
The Issue: Subpotent drug: Out of specification for assay of naloxone and buprenorphine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Dissolution Specifications: Out-of-specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.