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. 2,258 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,258 in last 12 months

Showing 4382143840 of 46,762 recalls

DrugMarch 14, 2013· Med Prep Consulting, Inc.

Recalled Item: Magnesium Sulfate 2 grams in Dextrose 5% for Injection Recalled by Med Prep...

The Issue: Non-Sterility; mold contamination

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 14, 2013· Med Prep Consulting, Inc.

Recalled Item: All Compounded Products Recalled by Med Prep Consulting, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility; potential for mold contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Seasonale(R) (Levonorgestrel/Ethinyl Estradiol Tablets) Recalled by Teva...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 14, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Camrese(TM) (Levonorgestrel/Ethinyl Estradiol Tablets) Recalled by Teva...

The Issue: Failed Impurity/Degradation Specifications; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 14, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products PHBR (Phenobarbital) Slides Recalled by...

The Issue: Ortho Clinical Diagnostics (OCD) received customer complaints of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2013· Synvasive Technology Inc

Recalled Item: The Oxford Partial Knee Recalled by Synvasive Technology Inc Due to Biomet...

The Issue: Biomet part # 506076, lot 928182 was received from Synvasive Technology...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Duraflo coated Femoral Cannula. Product Usage: The...

The Issue: Two unsealed pouches were found at an Edwards' distribution location in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2013· Elekta, Inc.

Recalled Item: Precise Treatment Table. To be used as part of radiation Recalled by Elekta,...

The Issue: The Column rotation can accidentally be moved to a different position which...

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

Class II — Potential Health HazardOngoing
FoodMarch 13, 2013· Daesang America Inc

Recalled Item: Sunchang Ssamjang Sesame and Garlic Seasoned Bean Paste 500 g Recalled by...

The Issue: Sesame and Garlic Flavored Mixed Soy Bean Paste contains peanut powder which...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 13, 2013· New Chapter, Inc.

Recalled Item: NewChapter Probiotic Elderberry Recalled by New Chapter, Inc. Due to...

The Issue: The product may contain an undeclared allergen soy

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 13, 2013· Epocal

Recalled Item: epoc BGEM Test Card (Catalogue number CT-1004-00-00). quantitative testing...

The Issue: This recall is being initiated because the affected lots of this product may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Separation Technology, Inc.

Recalled Item: SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE. Produce a monolayer of cells...

The Issue: Separation Technology, Inc. recalled SlidePrep Plus Cytology Centrifuges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Masimo Corporation

Recalled Item: Rad-8 Pulse Oximeters The Rad-8 family of pulse oximeters and Recalled by...

The Issue: Masimo has identified a very small number (0.02%) of Rad-8 devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Vitamin D Assay (100 tests) Recalled by Siemens Healthcare...

The Issue: Negative bias in patient samples for Vitamin D

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Vitamin D Assay (500 tests) Recalled by Siemens Healthcare...

The Issue: Negative bias in patient samples for Vitamin D

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Vitamin D Calibrator 2-pack Recalled by Siemens Healthcare...

The Issue: Negative bias in patient samples for Vitamin D

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Vitamin D Calibrator 6-pack Recalled by Siemens Healthcare...

The Issue: Negative bias in patient samples for Vitamin D

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Archer 0.035 inch (0.89mm) Super Stiff Guidewire Recalled by...

The Issue: Medtronic has identified an issue involving specific lot numbers of the...

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

Class II — Potential Health HazardOngoing
DrugMarch 12, 2013· L. Perrigo Co.

Recalled Item: Liothyronine Sodium Tablets Recalled by L. Perrigo Co. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: 3 month stability testing.

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

Class III — Low RiskOngoing
Refund
DrugMarch 12, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Jolessa (levonorgestrel/ethinyl estradiol) Tablets Recalled by Teva...

The Issue: Failed Tablet/Capsule Specifications: This recall is being carried out due...

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

Class III — Low RiskOngoing
Refund