Product Recalls in Hawaii

Product recalls affecting Hawaii — including food, drugs, consumer products, medical devices, and vehicles distributed to Hawaii. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,338 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,338 in last 12 months

Showing 3788137900 of 47,764 recalls

Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Arrow International Inc

Recalled Item: Arrow Select Kits (ASK) Recalled by Arrow International Inc Due to Certain...

The Issue: Certain product codes and lot numbers of Kits with Biopatch Dressing were...

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

Class III — Low RiskOngoing
DrugJanuary 8, 2015· Freedom Pharmaceuticals Inc

Recalled Item: 5-methyltetrahydrofolate Calcium (L) (a) 1 gm in 2 oz container Recalled by...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 8, 2015· Carestream Health, Inc.

Recalled Item: CS 8100 Recalled by Carestream Health, Inc. Due to Units device head...

The Issue: Units device head descended unexpectedly

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2015· Carestream Health, Inc.

Recalled Item: CS 8100 3D Recalled by Carestream Health, Inc. Due to Units device head...

The Issue: Units device head descended unexpectedly

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2015· GE Healthcare

Recalled Item: This correction applies to all GE Healthcare MRI systems with Recalled by GE...

The Issue: At certain sites, the MRU may not be connected to the magnet. In emergency...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 7, 2015· Cincinnati Sub-Zero Products Inc

Recalled Item: Cold Therapy Pad - cold water circulating pad Recalled by Cincinnati...

The Issue: Seals in the water path of the CT-99 cold therapy pad may separate during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: System 6 Aseptic Housing. The Stryker System 6 Aseptic Housings Recalled by...

The Issue: Stryker is recalling System 6 Aseptic Housing, due to a failed Continuous...

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

Class II — Potential Health HazardOngoing
DrugJanuary 6, 2015· American Health Packaging

Recalled Item: Benzonatate Capsules Recalled by American Health Packaging Due to Failed...

The Issue: Failed Tablet/Capsule Specifications; recall initiated by manufacturer due...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 5, 2015· Eillien's Candies, Inc.

Recalled Item: Walnut Pieces packaged in the following sizes and brand names: Recalled by...

The Issue: Product may be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 5, 2015· Clinical Innovations, LLC

Recalled Item: The Ebb Complete Tamponade System Recalled by Clinical Innovations, LLC Due...

The Issue: Clinical Innovations, LLC is voluntarily recalling the Ebb Complete...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2015· Arrow International Inc

Recalled Item: ARROW Epidural Needle Component (product number AN-05501). Epidural needles...

The Issue: The product labeling does not specify the 5 year shelf life of the product.

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

Class II — Potential Health HazardOngoing
FoodJanuary 3, 2015· Whole Foods Market

Recalled Item: Whole Foods Market Small Cookie Platter 18oz. Code: 24386800000 Recalled by...

The Issue: The firm is recalling Whole Foods Market Cookie Platter Small. Medium, and...

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

Class I — Serious Health HazardOngoing
Refund