Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,245 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,245 in last 12 months

Showing 4634146360 of 46,762 recalls

Medical DeviceMarch 22, 2012· Extremity Medical LLC

Recalled Item: Extremity Medical Recalled by Extremity Medical LLC Due to Lag screw...

The Issue: Lag screw measurement is short (approximately 5 mm) when using current screw...

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

Class II — Potential Health HazardOngoing
DrugMarch 16, 2012· Ranbaxy Inc.

Recalled Item: Balnetar Therapeutic Tar Bath Recalled by Ranbaxy Inc. Due to Subpotent...

The Issue: Subpotent (Single Ingredient Drug): out-of-specification result for coal tar...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 15, 2012· Sunquest Information Systems, Inc.

Recalled Item: Sunquest Laboratory Sunquest Laboratory is intended for use by professionals...

The Issue: Sunquest is recalling Sunquest Laboratory versions 6.1.0125 through...

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

Class II — Potential Health HazardOngoing
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