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 3650136520 of 47,764 recalls

DrugMay 13, 2015· West-Ward Pharmaceutical Corp.

Recalled Item: Fentanyl Citrate Inj. Recalled by West-Ward Pharmaceutical Corp. Due to...

The Issue: Failed Impurities/Degradation Specifications; 12 month stability testing...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 13, 2015· The Binding Site Group, Ltd.

Recalled Item: Optilite Analyser Recalled by The Binding Site Group, Ltd. Due to Potential...

The Issue: Potential risk of the Optilite lid/cover falling suddenly and causing injury...

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

Class II — Potential Health HazardOngoing
FoodMay 13, 2015· Mondelez International

Recalled Item: Outer carton : Nabisco Newtons Fig 24-2 OZ (56 g) Recalled by Mondelez...

The Issue: Fig Newtons brand Club Super Carton cookie products is mislabeled. The outer...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2015· Allegiant Health

Recalled Item: Famotidine Tablets Recalled by Allegiant Health Due to CGMP Deviations:...

The Issue: CGMP Deviations: Failure of the manufacturer, Wockhardt Ltd, to adequately...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 12, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: ReUnion TSA Shoulder System Recalled by Stryker Howmedica Osteonics Corp....

The Issue: A package labeled as Part #5901-S-4818, Lot MAC7C14, standard humeral head...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2015· Advanced Sterilization Products

Recalled Item: EVOTECH Endoscope Cleaner and Reprocessing System 220-230V Recalled by...

The Issue: Advanced Sterilization Products (ASP) is recalling the EVOTECH Endoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2015· Advanced Sterilization Products

Recalled Item: EVOTECH Endoscope Cleaner and Reprocessing System 208V Recalled by Advanced...

The Issue: Advanced Sterilization Products (ASP) is recalling the EVOTECH Endoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2015· Abbott Laboratories

Recalled Item: Alkaline Wash Recalled by Abbott Laboratories Due to The product is leaking...

The Issue: The product is leaking from the cap and crystallization was noted as present...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2015· Orthofix, Inc

Recalled Item: ORTHOFIX Centurion POCT System Drill Guide PN 69-1010 and PN Recalled by...

The Issue: There is a possibility that the thumb button remains in the depressed...

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

Class II — Potential Health HazardOngoing
DrugMay 11, 2015· Teva Pharmaceuticals USA

Recalled Item: Zebeta¿ (bisoprolol fumarate) Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Dissolution Specifications: OOS result during stability testing

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 8, 2015· Gyrus Acmi, Incorporated

Recalled Item: Gyrus ACMI Diego Elite Tubeset Recalled by Gyrus Acmi, Incorporated Due to...

The Issue: Potential lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: Shiley Neonatal Recalled by Covidien LP (formerly Nellcor Puritan Bennett...

The Issue: Reports where patients who recently switched from the current Shiley...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 8, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: Shiley Neonatal Recalled by Covidien LP (formerly Nellcor Puritan Bennett...

The Issue: Reports where patients who recently switched from the current Shiley...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 8, 2015· RAYSEARCH LABORATORIES AB

Recalled Item: RaySearch RayStation 2.5 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: RaySearch Laboratories AB became aware of an issue with the dose calculation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 0210-312-000-Woundcare Replacement kit with soft tip Recalled by Stryker...

The Issue: Potential sterility breach in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2015· Gyrus Acmi, Incorporated

Recalled Item: Gyrus ACMI Diego Elite Tubeset Recalled by Gyrus Acmi, Incorporated Due to...

The Issue: Potential lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2015· Ethicon, Inc.

Recalled Item: Ethicon Fast Absorbing Plain Gut - MultiPass Needles Recalled by Ethicon,...

The Issue: Ethicon Fast Absorbing Surgical Gut (Plain) Suture is being recalled because...

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

Class II — Potential Health HazardOngoing
FoodMay 8, 2015· Natural Creations Inc

Recalled Item: 250cc White Plastic Container containing 120 capsules Recalled by Natural...

The Issue: Natural Creations announces allergy alert and voluntary recall of New...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: LDL-Cholesterol plus gen.2. The Boehringer Mannheim Direct LDL-Cholesterol...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Uric Acid plus ver.2 In vitro test for the quantitative Recalled by Roche...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing