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. 2,642 recalls have been distributed to Alabama in the last 12 months.
Showing 7981–8000 of 28,641 recalls
Recalled Item: Medline Convenience kits labeled as: a. MAJOR VASCULAR CDS Recalled by...
The Issue: Kits contain leaking bottles of isopropyl alcohol
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Medline Product Name: convenience kits labeled as: LAP Recalled...
The Issue: Kits contain leaking bottles of isopropyl alcohol
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits labeled as: a. MIDDLE EAR PACK-LF Recalled by...
The Issue: Kits contain leaking bottles of isopropyl alcohol
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu VivaSight 2 DLT Recalled by Ambu Inc. Due to Firm has received...
The Issue: Firm has received complaints on the device concerning leak/rupture of either...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo Trak 21 Microcatheter Recalled by Stryker Neurovascular Due to...
The Issue: Microcatheter product label on the carton is missing the microcatheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Service manuals for the CT Recalled by GE Healthcare, LLC Due to As a result...
The Issue: As a result of unclear guidance in the service manual, the table can drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YelloPort Elite Universal Seal. For use in laparoscopic procedures. Recalled...
The Issue: There is the potential that YelloPort Elite Universal Seals packaging may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivo 45LS Ventilator- intended to provide continuous or intermittent...
The Issue: A forced shutdown of one of the processors did not generate a watch dog...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker INFINITY Resect Guide for INBONE Talus Recalled by Wright Medical...
The Issue: The instrument is incorrectly color coded.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DVR Anatomic Recalled by CHANGZHOU BIOMET MEDICAL DEVICES CO., LTD. Due to...
The Issue: One lot of DVRASL plates were incorrectly etched and may have been placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: GCX Channel Mounting Accessory Model/Catalog Number:...
The Issue: Under certain circumstances, the mounting screws may loosen or pull out from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Aisys CS2 Anesthesia System Recalled by GE Healthcare, LLC Due...
The Issue: There is a potential reversal of the O2 and air cylinder pressure transducer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 9B SP1. For radiation treatment planning. Recalled by RAYSEARCH...
The Issue: An issue with propagation of treatment course information from RayStation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM Test Card 25 Test Cards/box. In vitro diagnostic Recalled by...
The Issue: Discrepant (low bias) pO2 results, could be an incorrect diagnosis of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventana HE 600 System Recalled by Ventana Medical Systems Inc Due to There...
The Issue: There is a potential for fluid leak inside the Ventana HE 600 instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peak Universal Bond Self-Etch Bottle Kit Recalled by Ultradent Products,...
The Issue: SE primer may be missing some or all of the resin portion of the chemistry....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte 2301 2K 3.0 Ca 1 Mg Gal Recalled by Fresenius Medical Care...
The Issue: The product was potentially exposed to below-recommended storage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...
The Issue: Software related alarm escalation defect occurs after approximately 25 days...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuRx Diaphragm Pacing System (NeuRx DPS) Recalled by Synapse Biomedical Inc...
The Issue: Firm has revised labeling to consistently call out storage conditions and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaviCare Nurse Call/Voalte Nurse Call Recalled by Baxter Healthcare...
The Issue: An issue has been identified with Phillips (Emergin) and Longleaf non relay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.