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. 2,299 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,299 in last 12 months

Showing 3868138700 of 46,762 recalls

FoodSeptember 15, 2014· Gel Spice Co, Inc.

Recalled Item: Fresh Finds ground black pepper Net Wt. 3.53 oz (100g) Recalled by Gel Spice...

The Issue: Fresh Finds Black Pepper may contain Salmonella.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 14, 2014· Invivo Corporation

Recalled Item: Philips Expression Information Portal (IP5) Model 865471. The IP5 is...

The Issue: Frozen Display Numerics and Disabled Menu Keys after extended run time. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ and ADVIA Centaur¿ XP and ADVIA Centaur¿ CP Recalled by...

The Issue: Stability of the ADVIA Centaur Cleaning Solution is not assured

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

Class III — Low RiskOngoing
Medical DeviceSeptember 12, 2014· Eyemart Express Ltd

Recalled Item: Prescription eyeglass safety lenses. Vision correction Recalled by Eyemart...

The Issue: Prescription eyeglass safety lenses did not meet specifications.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Omni Micro-electrode/ electrode for cobas b221 analyzer. The Roche...

The Issue: The default for normal values are inconsistent between cobas b 221 and other...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 11, 2014· Abbott Ireland Diagnostics Division

Recalled Item: ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 Recalled by Abbott...

The Issue: 17% of ARCHITECT Total T3 Reagent Kit, LN 7K64-20/-25 reagent lots 38901UI00...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2014· Intuitive Surgical, Inc.

Recalled Item: ASSEMBLY Recalled by Intuitive Surgical, Inc. Due to Correction due to the...

The Issue: Correction due to the detection of a motor sensor failure in the Patient...

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

Class II — Potential Health HazardOngoing
FoodSeptember 11, 2014· Expo Fresh L.L.C

Recalled Item: Roma Tomatoes Recalled by Expo Fresh L.L.C Due to Potential Salmonella...

The Issue: Expo Fresh is recalling Roma Tomatoes because they have a potential to be...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 11, 2014· Hospira Inc.

Recalled Item: HEPARIN SODIUM Recalled by Hospira Inc. Due to Presence of Particulate...

The Issue: Presence of Particulate Matter: A particulate, confirmed as human hair, was...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 11, 2014· Qualitest Pharmaceuticals

Recalled Item: MethylPREDNISolone TABLETS Recalled by Qualitest Pharmaceuticals Due to...

The Issue: Subpotent; 6 month stability time point

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2014· Hospira Inc.

Recalled Item: Buprenorphine Hydrochloride Injection Recalled by Hospira Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specification: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 9, 2014· Zimmer, Inc.

Recalled Item: Persona The Personalized Knee System 2.5 mm Female Screw 48 Recalled by...

The Issue: The Persona 48mm X 2.5mm Female Screw is being recalled due to potential use...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: A zipser clamp is an instrument used to compress reduce Recalled by...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Xoran Technologies, LLC

Recalled Item: Xoran MiniCAT X-ray imaging device Recalled by Xoran Technologies, LLC Due...

The Issue: Out of tolerance kVp, Unexposed (black) frames, and Out of tolerance Dose.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: D'errico perforator drills are bone cutting and drilling instruments that...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: McKenzie enlarging burrs are bone cutting and drilling instruments that...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: Gardner-Wells traction tongs are skull tongs for traction used to Recalled...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: Hudson cranial drill sets (w/ brace and 5 attachments) are Recalled by...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: A uterine tenaculum is a hook-like instrument used to seize Recalled by...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: Schoitz weights are manual devices used with Schoitz tonometers and Recalled...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing