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. 1,034 recalls have been distributed to Alabama in the last 12 months.
Showing 21001–21020 of 50,591 recalls
Recalled Item: XP-XP Tibial Tray - Interlok 67 mm Item # 195753 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-CR Tibial Tray - Interlok 83 mm Item # 195277 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 73 mm Item # 195756 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Issues Scanning New Reagent Lot Test Definition on the Atellica IM 1300...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 83 mm Item # 195759 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-CR Tibial Tray - Interlok 91 mm Item # 195279 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-CR Tibial Tray - Interlok 79 mm Item # 195276 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9632 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard XP Tibial Tray 67 mm Item # 195247 Recalled by Zimmer Biomet, Inc....
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remisol Advance running on hardware with Windows XP Recalled by Normand-Info...
The Issue: A patch was released for a critical remote code execution vulnerability in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 91mm Item # 195761 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquilex Fluid Control System component: Bag deflector Recalled by WOM World...
The Issue: The deficit displayed by the pump can differ from the real deficit, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM anti-CCP IgG (aCCP) Assay Siemens Material Number: 10732998...
The Issue: Atellica IM anti-CCP IgG (aCCP) Test Definition (TDef) Mitigation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Conquest 40 PTA Dilation Catheter Recalled by Bard Peripheral Vascular...
The Issue: The catheter packaging incorrectly listed the balloon size as 8mm X 20mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RELPAX (eletriptan HBr) tablets Recalled by Pfizer Inc. Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: contamination with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EXACTAMED Oral Dispensers Recalled by Baxter Healthcare Corporation Due to...
The Issue: Exactamed 5 mL Oral Dispenser Pharmacy Packs may contain both 5 mL and 3 mL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AssayTip/AssayCup Tray-used on the cobas e 801 module which is Recalled by...
The Issue: AssayTips part of the AssayTip/AssayCup Tray Tips used on the cobas e 801...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZEUS ELISA Parvovirus B19 IgM Test System Recalled by Zeus Scientific, Inc....
The Issue: FDA inspection identified that due to increased positivity (false positives)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian Multileaf Collimator [MLC] Recalled by Varian Medical Systems, Inc....
The Issue: After a recent upgrade to the collimator software version 8.5, the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-HYDROCHLORIC ACID 2MG/ML INJ SOLN Recalled by First Royal Care Co. LLC,...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.