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. 2,377 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,377 in last 12 months

Showing 5016150180 of 50,591 recalls

DrugMarch 14, 2012· Zydus Pharmaceuticals USA Inc

Recalled Item: Metformin Hydrochloride Tablets Recalled by Zydus Pharmaceuticals USA Inc...

The Issue: Presence of Foreign Substance(s): A product complaint was received from a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 13, 2012· Advanced Sterilization Products

Recalled Item: STERRAD 200 System Carriage Recalled by Advanced Sterilization Products Due...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD 200 System...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek VAPR Hook Electrode 3.5mm Hook Electrode with Integrated...

The Issue: Product may have wrong large product identification label with symbols on...

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

Class II — Potential Health HazardOngoing
DrugMarch 9, 2012· Aurobindo Pharma LTD

Recalled Item: Northstar Zolpidem Tartrate Tablets USP 10 mg. Manufactured for Northstar RX...

The Issue: Adulterated Presence of Foreign Tablets: This product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2012· Pack Pharmaceuticals

Recalled Item: Ciprofloxacin Tablets Recalled by Pack Pharmaceuticals Due to Labeling...

The Issue: Labeling Illegible: Missing Label; The voluntary recall of the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 9, 2012· Princeton Biomeditech Corp

Recalled Item: Poly stat Flu A & B Test Manufactured for Polymedco Recalled by Princeton...

The Issue: There have been reports of dual positive (Flu A + Flu B positive) results...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2012· Princeton Biomeditech Corp

Recalled Item: Status Flu A + B Test Manufactured by Princeton Bio Recalled by Princeton...

The Issue: There have been reports of dual positive (Flu A + Flu B positive) results...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2012· Princeton Biomeditech Corp

Recalled Item: Orasure QuickFlu Rapid A+B Test Manufactured for OraSure Technologies...

The Issue: There have been reports of dual positive (Flu A + Flu B positive) results...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2012· Helix Medical LLC

Recalled Item: BLOM-SINGER indwelling TEP Occluder Recalled by Helix Medical LLC Due to...

The Issue: Helix Medical LLC is recalling the BLOM-SINGER indwelling TEP Occluder due...

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

Class III — Low RiskOngoing
Medical DeviceMarch 7, 2012· DePuy Orthopaedics, Inc.

Recalled Item: Pinnacle Hip Solutions ALTRX Polyethylene Acetabular Liner Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. (DePuy) is issuing a voluntary recall of one lot of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2012· Abbott Point Of Care Inc.

Recalled Item: i-STAT cTnI cartridges Product Usage: The i-STAT cTnl test is Recalled by...

The Issue: Abbott Point of Care has determined that i-Stat CTNL cartridges have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2012· Aesculap Implant Systems LLC

Recalled Item: S4 Cervical (S4C) Revision Instruments (FW099R and FW101R). The S4C Recalled...

The Issue: Aesculap Implant Systems, LLC has initiated a voluntary removal of the S4...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Quasar Nuclear Medicine System Recalled by GE Healthcare, LLC...

The Issue: Accelerated fatigue of the lateral axis motion subsystem of the Infinia...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2012· Becton Dickinson & Company

Recalled Item: BD Vacutainer PST Gel and Lithium Heparin (LH) Recalled by Becton Dickinson...

The Issue: BD is conducting a recall of the BD Vacutainer Plus Plastic Plasma Separator...

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

Class III — Low RiskOngoing
Medical DeviceMarch 1, 2012· Abbott Point Of Care Inc.

Recalled Item: I-STAT PT/INR cartridge Abbott Point of Care Inc. Abbott Park Recalled by...

The Issue: The i-STAT PT/INR cartridges have the potential to exhibit incorrectly...

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

Class II — Potential Health HazardOngoing
DrugFebruary 24, 2012· Lloyd Inc

Recalled Item: Thyro-Tab.075 mg. Recalled by Lloyd Inc Due to Subpotent (Single Ingredient...

The Issue: Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2012· Lloyd Inc

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc Due to...

The Issue: Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 24, 2012· BRAEMAR, INC.

Recalled Item: Lithium Thionyl non-rechargeable disposable battery pack P/N 350-0294-01...

The Issue: Braemar has recently became aware of a battery related incident that...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens syngo.plaza. Radiological image processing system Recalled by...

The Issue: Siemens became aware of a potential malfunction when using syngo.plaza with...

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

Class II — Potential Health HazardOngoing
DrugFebruary 23, 2012· www.vitaminbestbuy.com

Recalled Item: Man King Capsules Recalled by www.vitaminbestbuy.com Due to Marketed Without...

The Issue: Marketed Without an Approved ANDA/NDA: presence of sildenafil.

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

Class I — Serious Health HazardOngoing
Refund