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. 2,326 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,326 in last 12 months

Showing 3430134320 of 46,762 recalls

Medical DeviceSeptember 16, 2015· LifeHealth, LLC

Recalled Item: CC cartridges for IRMA TRUPOINT Blood Gas Analyzer Recalled by LifeHealth,...

The Issue: May report values outside the published performance specifications for pH....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2015· LifeHealth, LLC

Recalled Item: BG cartridges for IRMA TRUPOINT Blood Gas Analyzer Recalled by LifeHealth,...

The Issue: May report values outside the published performance specifications for pH....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2015· GE Healthcare

Recalled Item: Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is Recalled by...

The Issue: Images may be missing when a system parameter MapRoute is set to a value...

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

Class II — Potential Health HazardOngoing
FoodSeptember 15, 2015· Kermit, Inc.

Recalled Item: Kermit's Key Lime Cocktail Sauce Recalled by Kermit, Inc. Due to Undeclared Soy

The Issue: Undeclared soy on product label

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 15, 2015· Kermit, Inc.

Recalled Item: Kermit's Hot & Spicy Key Lime Barbecue Sauce Recalled by Kermit, Inc. Due to...

The Issue: Undeclared soy on product label

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 15, 2015· Kermit, Inc.

Recalled Item: Kermit's P4 Hot Sauce Recalled by Kermit, Inc. Due to Undeclared Soy

The Issue: Undeclared soy on product label

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 15, 2015· Kermit, Inc.

Recalled Item: Kermit's Sweet & Tasty Key Lime Barbecue Sauce Recalled by Kermit, Inc. Due...

The Issue: Undeclared soy on product label

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 15, 2015· Kermit, Inc.

Recalled Item: Kermit's Key Lime Ginger Wasabi Marinade Recalled by Kermit, Inc. Due to...

The Issue: Undeclared soy and wheat on product label

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 15, 2015· Kermit, Inc.

Recalled Item: Kermit's Key Lime Steak Sauce Recalled by Kermit, Inc. Due to Undeclared Soy

The Issue: Undeclared soy on product label

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 15, 2015· Kermit, Inc.

Recalled Item: Kermit's Chipotle Key Lime Barbecue Sauce Recalled by Kermit, Inc. Due to...

The Issue: Undeclared soy on product label

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 15, 2015· Kermit, Inc.

Recalled Item: Kermit's Medium Mannered Key Lime Barbecue Sauce Recalled by Kermit, Inc....

The Issue: Undeclared soy on product label

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 15, 2015· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Medical Device Identification Card for SureScan pacemaker...

The Issue: Some Medical Device Identification Cards provided to SureScan pacemaker...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Biochemical Diagnostics Inc

Recalled Item: CONSULT(TM) diagnostics hCG CONTROLS Kit Recalled by Biochemical Diagnostics...

The Issue: CONSULT diagnostics hCG Controls have discrepant storage temperatures listed...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 14, 2015· CooperSurgical, Inc.

Recalled Item: MILEX PESSARY KIT Recalled by CooperSurgical, Inc. Due to The products have...

The Issue: The products have been identified to have incorrect size prints on the MILEX...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Computed Tomography X-ray systems. Intended to produce...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray systems. Intended to produce...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 16-Slice (Air) Computed Tomography X-ray systems. Intended to...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore (Oncology & Radiology) Computed Tomography X-ray...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Flex Computed Tomography X-ray systems. Intended to produce...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems. Intended to produce...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing