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.
Showing 24981–25000 of 28,641 recalls
Recalled Item: PRE1055: Prevena Dressing Recalled by KCI USA, INC. Due to Prevena...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gelzone Shoulder Sleeve Recalled by Implantech Associates Inc Due to...
The Issue: Implantech initiated the voluntary recall of Gelzone Shoulder Sleever,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Certain Silicone TECNIS IOLs may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accessory shorts for the AlterG Anti-Gravity treadmill. Use with the...
The Issue: Unapproved material used by vendor in subset of shorts causing them to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Dynamics Picture Archiving and Communication System (PACS). Model...
The Issue: Potential patient data mixup. Improper error handling could allow for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Recalled by Cardiovascular Systems, Inc. Due to Cardio vascular Systems...
The Issue: Cardio vascular Systems Inc. has initiated a recall to request the immediate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 3.2 mm Guide Wire 400mm. Used for guiding the Recalled by Synthes,...
The Issue: Synthes 3.2 mm Guide Wire 400mm included an incorrect raw material listed on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Notch Titanium Reconstructive Plate Product Usage: The Synthes...
The Issue: Certain modules containing the Synthes Small Notch Titanium Reconstructive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum XL3 Multi line Infusion System Recalled by Hospira Inc. Due to There is...
The Issue: There is the potential for the door roller assembly on the Plum LifeCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeCare 5000 Pump (Plum 1.6) infusion pump Recalled by Hospira Inc. Due to...
The Issue: There is the potential for the door roller assembly on the Plum LifeCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RetCam 3 Recalled by Clarity Medical Systems Inc Due to Software anomaly for...
The Issue: Software anomaly for RetCam 3, RetCam Shuttle and RetCam Portable with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum XL Recalled by Hospira Inc. Due to There is the potential for the door...
The Issue: There is the potential for the door roller assembly on the Plum LifeCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Kodak 2200 Intraoral X-Ray System Recalled by Carestream Health Inc....
The Issue: Carestream received problem reports relating to apparent early failure of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow-B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling
The Issue: Mislabeled product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Kodak 2100 Intraoral X-Ray System Recalled by Carestream Health Inc....
The Issue: Carestream received problem reports relating to apparent early failure of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaSure Impedance Controlled Endometrial Ablation System Radiofrequency...
The Issue: NovaSure Radiofrequency Control Units may not meet a requirement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Model: 861290 The HeartStart...
The Issue: HeartStart XL+ battery charge time to 100% capacity at 35¿C (95¿F) is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable Clip Applier Manufactured by AtriCure Recalled by Atricure Inc Due...
The Issue: The firm was notified by a customer of a cracked spring in the handle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartSite Needleless Connector Recalled by CareFusion 303, Inc. Due to...
The Issue: CareFusion is recalling the SmartSite Needlefree Connector, model number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buzzaround XL scooters' Product Usage: mobility Recalled by Golden...
The Issue: Buzzaround XL scooters' front to rear lockup can become unintentionally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.