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. 1,813 recalls have been distributed to Alabama in the last 12 months.
Showing 36481–36500 of 50,591 recalls
Recalled Item: NAMIC CONVENIENCE KIT HOLYOKE HOSPITAL SPECIAL PROCEDURE KIT Recalled by...
The Issue: Procedure Products initiated the recall due to the inner lumen of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS HM3000 Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA CLI V3.X TO V4.1 DL380 SERVER Product Usage: MYLA Recalled by...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA CLINIC PATCH 3.3.0 CD Product Usage: MYLA is a Recalled by bioMerieux,...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...
The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA MASTER DVD V4.1 CLI Product Usage: MYLA is a Recalled by bioMerieux,...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA MASTER DVD V4.0 CLI Product Usage: MYLA is a Recalled by bioMerieux,...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optisure Dual Coil Defibrillation Leads Recalled by St Jude Medical Cardiac...
The Issue: Leads may have been compromised during the manufacturing process, with cuts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS V3000 Recalled by Philips Electronics North America Corporation Due...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10 Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS CV Recalled by Philips Electronics North America Corporation Due to...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/10 Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 OR Table Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS Allura 15-12 (biplane) Recalled by Philips Electronics North...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue CIC-C1q EIA Recalled by Diagnostic Hybrids, Inc. Due to A component...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue SC5b-9 Plus EIA (RUO) Recalled by Diagnostic Hybrids, Inc. Due to A...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue SC5b-9 Plus EIA (CE-IVD) Recalled by Diagnostic Hybrids, Inc. Due...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod¿ Recalled by Insulet Corporation Due to Pod's needle mechanism fails...
The Issue: Pod's needle mechanism fails to deploy or there is a delay in the deployment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS 4674 Custom Pack. For use in a general clinical procedure. Recalled by...
The Issue: AMS 4674 Custom Pack is recalled because this kit containing U-SDN 2 Part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.