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 4190141920 of 46,762 recalls

Medical DeviceAugust 13, 2013· Codman & Shurtleff, Inc.

Recalled Item: MedStream Kit (6 units) Recalled by Codman & Shurtleff, Inc. Due to Drug...

The Issue: Drug flow rates exceeding programmed flow rates.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 12, 2013· Cordis Corporation

Recalled Item: Cordis ADROIT 6F Guiding Catheter Product Usage: For intravascular...

The Issue: Due to a labeling error related to the conversion of the inner diameter of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2013· Siemens Healthcare Diagnostics

Recalled Item: ADVIA 2120/2120i Hematology Systems with ADVIA Autoslide connected to it...

The Issue: Siemens determined that if an autosampler rack jam error occurs during...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2013· MicroAire Surgical Instruments, LLC

Recalled Item: Steinmann Pin Recalled by MicroAire Surgical Instruments, LLC Due to A...

The Issue: A medical device used in surgical procedures was packaged in a pouch in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal (R) Surgical Eye Spears Recalled by DeRoyal Industries Inc Due to...

The Issue: One lot of eye spears was labeled as being x-ray detectable, but contained...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2013· Churchill Medical Systems, Inc.

Recalled Item: Central Dressing Change Kit Recalled by Churchill Medical Systems, Inc. Due...

The Issue: Microbore tubing disconnecting from male luers on the extension sets.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2013· Abbott Laboratories, Inc

Recalled Item: Clinical Chemistry Phosphorus Reagent The Phosphorus assay is used for...

The Issue: Reagent lots 64736UN12, 03991UN13, 51611UN13, 74805UN12, and 03992UN13 have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: T8 REMOVAL HEAD Recalled by Medtronic Sofamor Danek USA Inc Due to One lot...

The Issue: One lot of the T8 Removal Head had incorrect hardness specification, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2013· Churchill Medical Systems, Inc.

Recalled Item: Vygon 14 Microbore Extension Set with Bionector Recalled by Churchill...

The Issue: Microbore tubing disconnecting from male luers on the extension sets.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2013· MicroAire Surgical Instruments, LLC

Recalled Item: Kirschner-Wire (K-Wire) Recalled by MicroAire Surgical Instruments, LLC Due...

The Issue: A medical device used in surgical procedures was packaged in a pouch in...

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

Class II — Potential Health HazardOngoing
DrugAugust 12, 2013· Jack Rabbit, Inc

Recalled Item: J.R. Jack Rabbit All Natural Herbal Supplement Recalled by Jack Rabbit, Inc...

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 12, 2013· Terri Lynn Inc.

Recalled Item: Mixed nuts in a plastic bag labeled in part: PREMIUM QUALITY Recalled by...

The Issue: Terri Lynn Inc. "Deluxe Mixed Nuts No Peanuts" was found to have undeclared...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 12, 2013· Terri Lynn Inc.

Recalled Item: Mixed nuts in a plastic bag labeled in part: Deluxe Mixed Nuts with...

The Issue: Terri Lynn Inc. "Deluxe Mixed Nuts No Peanuts" was found to have undeclared...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 9, 2013· Dove Chocolate Discoveries Llc

Recalled Item: Dove Chocolate Discoveries Fruit Collection Dark Chocolate - Covered...

The Issue: Cinnamon Dusted Dark Chocolate Almonds (Item Number: 3059D) were packaged in...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 9, 2013· Specialty Compounding, LLC

Recalled Item: All products Recalled by Specialty Compounding, LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2013· Specialty Compounding, LLC

Recalled Item: CALCIUM GLUCONATE 2 gm (PF) PRESERVATIVE FREE in 100 mL Recalled by...

The Issue: Non Sterility: Microbial contamination

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 9, 2013· Varian Medical Systems, Inc.

Recalled Item: VARISOURCE Breast Template System for high-dose rate Brachytherapy....

The Issue: The recall was initiated after Varian Medical became aware the Lexan...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2013· OPTI Medical Systems, Inc

Recalled Item: Model BP7507 OPTI LION E-Plus Cassettes 25 Cassettes with Sample Probes...

The Issue: OPTI LION E-Plus Cassettes were labeled with an incorrect barcode. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2013· Sonogage Inc

Recalled Item: Sonogage EyeScan Recalled by Sonogage Inc Due to During an FDA inspection on...

The Issue: During an FDA inspection on 7/15-26/2013, it was discovered that the firm...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2013· Philips Healthcare Inc.

Recalled Item: Philips Easy Upgrade DR Recalled by Philips Healthcare Inc. Due to The...

The Issue: The mirror icon on the bottom of each image could be misinterpreted as a...

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

Class II — Potential Health HazardOngoing