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 3858138600 of 46,762 recalls

Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7002 Part Number: MRI-02 MRI-Arm Sleeve Various Sizes...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7007 Part Number: MRI-07 MRI-Breast Shield Product Usage:...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7004 Part Number: MRI-04 MRI-Poncho Product Usage: Radio...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Microbiologics Inc

Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to This strain should be...

The Issue: This strain should be resistant to high levels of Gentamicin and be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Microbiologics Inc

Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to This strain should be...

The Issue: This strain should be resistant to high levels of Gentamicin and be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Microbiologics Inc

Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to This strain should be...

The Issue: This strain should be resistant to high levels of Gentamicin and be...

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

Class II — Potential Health HazardOngoing
DrugOctober 3, 2014· Wisconsin Pharmacal Company

Recalled Item: CVS pharmacy Recalled by Wisconsin Pharmacal Company Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: CVS Pharmacy Pain Relieving...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2014· Sagent Pharmaceuticals Inc

Recalled Item: Ketorolac Tromethamine INJECTION Recalled by Sagent Pharmaceuticals Inc Due...

The Issue: Incorrect or Missing Lot and/or Exp Date: Ketorolac Tromethamine Injection,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 3, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips Avalon Monitors with software revision J.30.58: Model Product FM20...

The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips IntelliVue Monitors with software revisions J.21.03 Recalled by...

The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2014· Zimmer, Inc.

Recalled Item: Natural Knee II Revision Femoral Stem Recalled by Zimmer, Inc. Due to Failed...

The Issue: Failed to meet established requirements for sterile barrier integrity due to...

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

Class II — Potential Health HazardOngoing
DrugOctober 2, 2014· Valeant Pharmaceuticals International

Recalled Item: Locoid (hydrocortisone butyrate 0.1%) Recalled by Valeant Pharmaceuticals...

The Issue: Subpotent Drug; for the active, HCB, and preservatives, Propylparaben and...

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

Class III — Low RiskOngoing
Refund
DrugOctober 2, 2014· Valeant Pharmaceuticals International

Recalled Item: Hydrocortisone Butyrate Cream 0.1% Recalled by Valeant Pharmaceuticals...

The Issue: Subpotent Drug; for the active, HCB, and preservatives, Propylparaben and...

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

Class III — Low RiskOngoing
Refund
DrugOctober 2, 2014· Sandoz, Inc

Recalled Item: candesartan cilexetil Recalled by Sandoz, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: An Out of Specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugOctober 1, 2014· Hospira Inc.

Recalled Item: Hydromorphone Hydrochloride Injection Recalled by Hospira Inc. Due to Lack...

The Issue: Lack Of Assurance Of Sterility: Confirmed customer complaints of glass...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 1, 2014· Avella of Deer Valley, Inc.

Recalled Item: HYDROXYPROGESTERONE CAPROATE 250 MG/ML (IN SESAME OIL) Recalled by Avella of...

The Issue: Crystallization: Formation of crystals observed in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 1, 2014· Zydus Pharmaceuticals USA Inc

Recalled Item: Amlodipine Besylate Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Discoloration: Brown spots were noted embedded in Amlodipine Besylate...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 1, 2014· Zimmer, Inc.

Recalled Item: Continuum Acetabular System Trabecular Metal Shell with Multi Holes Recalled...

The Issue: The affected products are missing polar boss threads.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Medartis, Inc.

Recalled Item: APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Recalled...

The Issue: A recall of the APTUS Ulna Shortening 2.5 instrument was initiated due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Roscoe Medical Inc

Recalled Item: Transport Rollator with Padded Seat Recalled by Roscoe Medical Inc Due to...

The Issue: The caster may separate completely from the device frame causing injury to user.

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

Class II — Potential Health HazardOngoing