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. 2,384 recalls have been distributed to Alabama in the last 12 months.
Showing 45201–45220 of 50,591 recalls
Recalled Item: Ciprofloxacin Tablets Recalled by Mylan Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Besylate and Benazepril HCl Capsules Recalled by Mylan...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxycodone and Acetaminophen Tablets Recalled by Watson Laboratories Inc Due...
The Issue: Presence of Foreign Tablets/Capsules: 20 tablets of Oxycodone/APAP 7.5/500...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Recalled by CooperSurgical,...
The Issue: CooperSurgical is recalling two lots of 900-863 because the wrong package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Nex Healing Abutment Recalled by Southern Implants, Inc Due to Southern...
The Issue: Southern Implants is recalling the Tri-Nex healing abutment because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: pH 7.0 Buffer Solution Pint and Quart Bottles Recalled by Mesa Laboratories,...
The Issue: Mesa Laboratories, Inc. is recalling certain lots of pH 7.0 Buffer Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NX3 Try-In Gel. The product is used as a tooth shade resin material....
The Issue: Kerr Corporation is voluntarily recalling one lot of NX3 Try-In Gel, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roasted Salted Mixed Nuts w/ Peanuts Recalled by Dutch Valley Food...
The Issue: Roasted Salted Mixed Nuts with Peanuts were recalled for undeclared tree...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Honey Roasted Peanuts Recalled by Dutch Valley Food Development Inc. Due to...
The Issue: Honey Roasted Peanuts were recalled due to undeclared milk (lactose) and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the Access 2 Immunoassay System because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAQUET Getinge Group CARDIOHELP Base Unit .7999 .8012 Recalled by Maquet...
The Issue: It has come to the attention of MAQUET that in certain rare instances, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Loratadine 24 HR-OTC Recalled by Physicians Total Care, Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Affected lot numbers may contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Risperdal CONSTA (risperiDONE) Recalled by Janssen Pharmaceuticals, Inc. Due...
The Issue: Non-Sterility: Janssen is recalling one lot of Risperdal CONSTA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Artis zee / zeego Angiography System is designed as Recalled by Siemens...
The Issue: There is a potential issue on running Artis systems running software VC1x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rotoprone therapy System is an advanced patient care system Recalled by...
The Issue: The lock pin can become stuck in the "in" position during the manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harvest Graft Delivery System Recalled by Harvest Technologies Corporation...
The Issue: Potential for leur connector to leak or have cracks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P21x/5-1 MHz transducer Recalled by SonoSite, Inc. Due to FUJIFILM SonoSite...
The Issue: FUJIFILM SonoSite Inc. remove P21x/5-1 Transducer because the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hospira RECEPTAL LINERS: 1L(1000mL) Recalled by Hospira Inc. Due to Hospira...
The Issue: Hospira has become aware of customers using the incorrect size Receptal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hospira RECEPTAL CANISTERS: 1L(1000mL) Recalled by Hospira Inc. Due to...
The Issue: Hospira has become aware of customers using the incorrect size Receptal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.