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. 2,245 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,245 in last 12 months

Showing 4626146280 of 46,762 recalls

Medical DeviceApril 17, 2012· ICU Medical, Inc.

Recalled Item: 94" (239cm) 20 Drop Admin Set w/High Pressure 4-Way (300 psi) Stopcock...

The Issue: The firm initiated the recall due to a molding defect in a high pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2012· ICU Medical, Inc.

Recalled Item: High Pressure Stopcock (3-Way Recalled by ICU Medical, Inc. Due to The firm...

The Issue: The firm initiated the recall due to a molding defect in a high pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2012· ICU Medical, Inc.

Recalled Item: Flush Kit w 3 Way Off Stopcock Product Usage: Flush Kit Recalled by ICU...

The Issue: The firm initiated the recall due to a molding defect in a high pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2012· ICU Medical, Inc.

Recalled Item: Cardiac Catheterization Waste Management System w/1000mL Waste Bag Recalled...

The Issue: The firm initiated the recall due to a molding defect in a high pressure...

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

Class II — Potential Health HazardOngoing
DrugApril 16, 2012· Bracco Diagnostics Inc

Recalled Item: Bracco Diagnostics multihance (gadobenate dimeglumine) injection Recalled by...

The Issue: Short Fill: The product is being recalled due to a potential underfill of...

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

Class III — Low RiskOngoing
Refund
DrugApril 16, 2012· Bracco Diagnostics Inc

Recalled Item: Multihance Multipack (gadobenate dimeglumine) injection Recalled by Bracco...

The Issue: Lack of Assurance of Sterility; Product recalled due to displacement of the...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 16, 2012· Hong Lee Trading Inc

Recalled Item: Preserved Apricots -- NET WEIGHT 300gr (10.6oz) -- Ingredient: Salt Recalled...

The Issue: The product contained undeclared sulfites (108.8 ppm) and undeclared Yellow...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 16, 2012· Berchtold Corp.

Recalled Item: OPERON D850 Surgical Table Product Usage: Surgical Table Recalled by...

The Issue: Table was not lowering.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2012· Maquet Medical Systems, Usa

Recalled Item: Maquet Getinge Group Operating Table System Magnus Carbon-Fibre Table Top...

The Issue: As a result of a small number of customer complaints, MAQUET conducted an...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2012· Varian Medical Systems, Inc.

Recalled Item: Rectal Retractors Recalled by Varian Medical Systems, Inc. Due to A medical...

The Issue: A medical device used in brachytherapy may become contaminated and can cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2012· Varian Medical Systems, Inc.

Recalled Item: Rectal Retractors Recalled by Varian Medical Systems, Inc. Due to A medical...

The Issue: A medical device used in brachytherapy may become contaminated and can cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2012· Becton Dickinson & Co.

Recalled Item: BD Gram Stain Kit Recalled by Becton Dickinson & Co. Due to Potential for...

The Issue: Potential for increase level of artifacts to appear as large, spherical and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2012· Becton Dickinson & Co.

Recalled Item: Gram Crystal Violet 250 mL Recalled by Becton Dickinson & Co. Due to...

The Issue: Potential for increase level of artifacts to appear as large, spherical and...

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

Class II — Potential Health HazardOngoing
DrugApril 11, 2012· Hospira, Inc.

Recalled Item: Propofol Injectable Emulsion Recalled by Hospira, Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: A single visible particulate was observed in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 11, 2012· Siemens Medical Solutions USA, Inc.

Recalled Item: E.CAM emission computed tomography system used to detect or image Recalled...

The Issue: Radial motor drives replaced during a customer service action were...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2012· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia E is a multi-purpose SPECT system used to detect Recalled by Siemens...

The Issue: Radial motor drives replaced during a customer service action were...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2012· Beckman Coulter Inc.

Recalled Item: AutoMate 1250 and AutoMate 2550 Recalled by Beckman Coulter Inc. Due to The...

The Issue: The recall was initiated because Beckman Coulter has confirmed customer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2012· Kerr Corporation

Recalled Item: The brand name of the device is Laser Loupes Recalled by Kerr Corporation...

The Issue: The firm initiated the recall for Laser Loupes because the ink used to mark...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

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
DrugApril 9, 2012· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddy's Amlodipine Besylate and Benazepril Hydrochloride 5 mg*/20 mg...

The Issue: Adulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has...

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

Class II — Potential Health HazardOngoing
Refund