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. 2,283 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,283 in last 12 months

Showing 4156141580 of 46,762 recalls

FoodSeptember 20, 2013· Threshold Enterprises Ltd

Recalled Item: Serene Science/Source Naturals brand GABA (Gamma-Aminobutyric Acid) Recalled...

The Issue: The firm found small piece of metal fragment in one tablet during its...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 20, 2013· Medrad Inc dba Bayer R&I

Recalled Item: MEDRAD¿ Stellant CT Injector System with Certegra Workstation Recalled by...

The Issue: The root cause investigation showed that the under-volume hazard can occur...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2013· Midmark Corp dba Progeny Inc

Recalled Item: The Vantage Digital Panoramic System delivers high-value features standard...

The Issue: An error was identified in the Real Time Controller (RTC) firmware versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2013· Aesculap, Inc.

Recalled Item: Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)...

The Issue: The trial insertion instrument may disassemble during use due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2013· Maquet Cardiovascular, LLC

Recalled Item: Ultima OPCAB System Recalled by Maquet Cardiovascular, LLC Due to MAQUET has...

The Issue: MAQUET has identified a potential issue with the ULTIMA OPCAB (part numbers...

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

Class II — Potential Health HazardOngoing
DrugSeptember 19, 2013· Ferring Pharmaceuticals Inc

Recalled Item: ENDOMETRIN (progesterone) Vaginal Insert 100 mg USP Recalled by Ferring...

The Issue: Discoloration; due to prolonged heat exposure.

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 19, 2013· GE Healthcare, LLC

Recalled Item: Multi Absorber Original Recalled by GE Healthcare, LLC Due to GE Healthcare...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2013· GE Healthcare, LLC

Recalled Item: AW VolumeShare 4 (ADVANTAGE WORKSTATION 4.3.) Recalled by GE Healthcare, LLC...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2013· Atossa Genetics, Inc.

Recalled Item: Brand: The ForeCYTE Breast Health Test Recalled by Atossa Genetics, Inc. Due...

The Issue: Atossa Genetics is recalling ForeCYTE Breast Health Test, Mammary Aspiration...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2013· AGFA Corp.

Recalled Item: IMPAX 5.2 DB Server (running Oracle 10.1.0.4.0) Recalled by AGFA Corp. Due...

The Issue: System downtime and/or slow performance may result if software in use is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2013· Richard Wolf Medical Instruments Corp.

Recalled Item: Individual units labeled in part: Recalled by Richard Wolf Medical...

The Issue: Richard Wolf Medical Instrument Corporation recieved a complaint stating...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 100NX Cassettes The STERRAD Sterilization System is a low Recalled...

The Issue: Advanced Sterilization Products (ASP) is recalling the three lots (13F049,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2013· GE Healthcare Beijing , Hangwei Medical Systems, Co. LTD

Recalled Item: GE Brivo OEC715/785/865 C-Arm Recalled by GE Healthcare Beijing , Hangwei...

The Issue: GE is recalling certain lots of GE Brivo OEC715/785/865 C-Arm due to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 200 Sterilizer (Single Door) Recalled by Advanced Sterilization...

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

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

Class II — Potential Health HazardOngoing
DrugSeptember 17, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Institutional, Inc. (d.b.a....

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Institutional, Inc. (d.b.a....

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Institutional, Inc. (d.b.a....

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2013· Lupin Pharmaceuticals Inc.

Recalled Item: Quinapril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: During stability testing an...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2013· Lupin Pharmaceuticals Inc.

Recalled Item: Quinapril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: During stability testing an...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2013· Amgen, Inc.

Recalled Item: Prolia (denosumab) Injection Recalled by Amgen, Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Visible cellulose fibers were observed in a...

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

Class II — Potential Health HazardOngoing
Refund