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. 2,638 recalls have been distributed to Alabama in the last 12 months.
Showing 8581–8600 of 28,641 recalls
Recalled Item: BUTLER Clear Dip Recalled by Sunstar Americas, Inc. Due to Product lacks...
The Issue: Product lacks premarket clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Everest MI XT Inner Dilator Recalled by K2M, Inc Due to Stryker received two...
The Issue: Stryker received two (2) complaints for units from specific lots of Inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luscient Diagnostics 2nd Generation of COVID-19 Viral Antigen Test For...
The Issue: COVID-19 test kits (Antibody Rapid Test kit and Antigen Rapid Test Kit) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for small bone...
The Issue: During insertion of the middle phalanx implant into bone, the driver may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Cannulated Hammertoe Standard Instrument Kit-indicated for small bone...
The Issue: During insertion of the middle phalanx implant into bone, the driver may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LuSys 2nd Generation of COVID-19 Viral Antigen Test For all Recalled by...
The Issue: COVID-19 test kits (Antibody Rapid Test kit and Antigen Rapid Test Kit) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COVID-19 IgG/IGM Antibody Test For Detection of COVID-19 IgG and Recalled by...
The Issue: COVID-19 test kits (Antibody Rapid Test kit and Antigen Rapid Test Kit) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Everest MI XT Outer Dilator Recalled by K2M, Inc Due to Stryker received two...
The Issue: Stryker received two (2) complaints for units from specific lots of Inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Recalled by TELEFLEX MEDICAL INC Due...
The Issue: The firm received reports indicating PTD tip separation during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Recalled by TELEFLEX MEDICAL INC Due...
The Issue: The firm received reports indicating PTD tip separation during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 Fr. X 65 cm Arrow-Trerotola PTD Kit Recalled by TELEFLEX MEDICAL INC Due...
The Issue: The firm received reports indicating PTD tip separation during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device) Recalled by...
The Issue: The firm received reports indicating PTD tip separation during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device) Recalled by...
The Issue: The firm received reports indicating PTD tip separation during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Recalled by TELEFLEX MEDICAL INC Due...
The Issue: The firm received reports indicating PTD tip separation during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Recalled by TELEFLEX MEDICAL INC Due...
The Issue: The firm received reports indicating PTD tip separation during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RNAstill Molecular Transport Medium Vial Recalled by BASE 10 GENETICS INC...
The Issue: The product does not have 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Voyager Rollator-intended as a mechanical walker Model Number: RLEU10xx...
The Issue: Wheel spoke may crack causing the wheel to separate from the axle may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NavitrackER Kit A: Knee Recalled by Orthosoft, Inc. dba Zimmer CAS Due to...
The Issue: The product was released for distribution without passing sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Primary Shoulder Stem Recalled by Biomet, Inc....
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arcos Modular Revision Hip System Recalled by Biomet, Inc. Due to The...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.