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. 2,509 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,509 in last 12 months

Showing 2100121020 of 50,591 recalls

Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 63 mm Item # 195751 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 71 mm Item # 195249 Recalled by Zimmer Biomet, Inc....

The Issue: The locking bar not fully engaging

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 71 mm Item # 195755 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP- CR Tibial Tray- Interlok 59mm Item # 195268 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 87 mm Item # 195254 Recalled by Zimmer Biomet, Inc....

The Issue: The locking bar not fully engaging

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 87 mm Item # 195760 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 67mm Item # 195271 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 69mm Item # 195272 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 83 mm Item # 195253 Recalled by Zimmer Biomet, Inc....

The Issue: The locking bar not fully engaging

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

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.

Class II — Potential Health HazardOngoing
DrugAugust 14, 2019· Pfizer Inc.

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.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 14, 2019· Bard Peripheral Vascular Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2019· WOM World of Medicine AG

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2019· Siemens Healthcare Diagnostics, Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2019· Roche Diagnostics Operations, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2019· Baxter Healthcare Corporation

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.

Class III — Low RiskOngoing
DrugAugust 12, 2019· First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Recalled Item: S-GLUTATHIONE 200MG/3ML (PF) INHALATION SOLN Recalled by First Royal Care...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 12, 2019· First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Recalled Item: S-PYRIDOXINE HCL (B6) 100MG/ML MDV Recalled by First Royal Care Co. LLC, dba...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 12, 2019· First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Recalled Item: S-TEST CYP/PROP/DECA-NAN 250MG/ML (80/10/10) IN SESAME OIL Recalled by First...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund