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. 2,680 recalls have been distributed to Alabama in the last 12 months.
Showing 2161–2180 of 28,641 recalls
Recalled Item: C-SECTION PPS Recalled by American Contract Systems Inc Due to ACS is unable...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AV FISTULA Recalled by American Contract Systems Inc Due to ACS is unable to...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THORACIC PACK Recalled by American Contract Systems Inc Due to ACS is unable...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: Beckman Coulter identified that an issue for DxI 9000 tip stocker interface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis: Anesthesia Station ES Recalled by CareFusion 303, Inc. Due to Sync...
The Issue: Sync timeout may occur between the server and automated dispensing device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPEN HEART A PACK Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CV BASIC PUMP PACK Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAJOR DIEP Recalled by American Contract Systems Inc Due to ACS is unable to...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPINE LUMBAR PACK Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEURO IR TRAY Recalled by American Contract Systems Inc Due to ACS is unable...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EAR PACK Recalled by American Contract Systems Inc Due to ACS is unable to...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAPAROSCOPY PACK Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAPAROSCOPY PACK Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TOTAL HIP PACK Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AURORA Surgiscope System Recalled by Integra LifeSciences Corp. Due to...
The Issue: Possibility for the obturator to break (separate).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDITECH Expanse Laboratory (LAB) Recalled by Medical Information...
The Issue: Entering multiple keys that trigger input simultaneously may remove data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: the DxI 9000 encoder wheel was misaligned on the motor shaft, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access 2 Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due to...
The Issue: Beckman Coulter identified that an issue for Access 2 Sample Motors (B48016)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA Recalled by...
The Issue: Unexpected loose material in the male luer used in the aortic root cannula...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotarex Atherectomy System and Instructions for Use Recalled by Bard...
The Issue: Atherectomy Catheter eIFU updated to clarify and emphasize procedural steps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.