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. 2,483 recalls have been distributed to Alabama in the last 12 months.
Showing 22161–22180 of 28,641 recalls
Recalled Item: Sorin Stockert Heater-Cooler 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Potential colonization of organisms, including Mycobacteria, in Sorin Heater...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorin Stockert Heater-Cooler 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Potential colonization of organisms, including Mycobacteria, in Sorin Heater...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Block Versions Used by Dental Offices often to as Recalled by 3M Company -...
The Issue: 3M is initiating a Field Correction to remove the crown indication from all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-Stat PT/INR Cartridges List number 03P89-24 The cartridges are packaged...
The Issue: Certain lots of PT/INR cartridges may generate a higher than typical number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPD-Scan III Power/Corneal Analyzer Opthalmic Software versions 1.00.08...
The Issue: Software bug was found where there was no difference in Total and Corneal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASP-1020 LipoTower with Aspiration Pump. Medical use. Recalled by MicroAire...
The Issue: There is potential risk of electrical shock if lead wires inside the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use....
The Issue: There is potential risk of electrical shock if lead wires inside the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement...
The Issue: Incorrect product label. The type of Sewing Ring was mislabeled as being a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OxySure Model 615 disposable replacement cartridges Recalled by Oxysure...
The Issue: Flow rate of the recalled replacement cartridges does not meet the draft FDA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE CONV FB CR TB TRL SZ3 - 10 INTENDED Recalled by DePuy Orthopaedics,...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE RP CR ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Recalled by...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE RP PS ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Recalled by...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro...
The Issue: QC results were out of range resulting in false resistant strains.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D Classical R & F system. Recalled by GE...
The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D and Advantx Legacy/Legacy-D Radiographic and...
The Issue: The SFD/IDD safety mechanism may not engage properly at the lower range of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to A reported incident of a...
The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE CONV FB CR ARTICULATION SURFACE SZ1 INTENDED USE: The Recalled by...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE CONV RP PS ARTICULATION SURFACE SZ1-9 INTENDED USE: The Recalled by...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE FB CR ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Recalled by...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE FB PS ARTICULATION SURFACE SIZES 3-8 INTENDED USE: The Recalled by...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.