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. 941 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
941 in last 12 months

Showing 39681–39700 of 47,764 recalls

FoodJuly 25, 2014· Florimont, Inc.

Recalled Item: Tiny Isle Chocolate Truffles Macadamia Nut: Gluten Free Recalled by...

The Issue: Candy was made using carob powder that is currently under recall by the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 25, 2014· Florimont, Inc.

Recalled Item: Tiny Isle Chocolate Truffles Mint Crunch: Gluten Free Recalled by Florimont,...

The Issue: Candy was made using carob powder that is currently under recall by the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 25, 2014· GE Healthcare, LLC

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

The Issue: GE Healthcare has become aware of a potential safety issue involving the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2014· Galt Medical Corporation

Recalled Item: GALT VALVED TEARAWAY INTRODUCER SET GALT VTI RX ONLY UNITS Recalled by Galt...

The Issue: The adhesive used in the product could dislodge when objects are inserted...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2014· Galt Medical Corporation

Recalled Item: GALT VALVED TEARAWAY KIT GALT VTI w/ Sideport Stainless Steel Recalled by...

The Issue: The adhesive used in the product could dislodge when objects are inserted...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2014· OrthoPediatrics Corp

Recalled Item: ACL Sleeve Installation Tool Sizes: 6mm Recalled by OrthoPediatrics Corp Due...

The Issue: Weld fractures on the Sleeve Installation Tool for ACL reconstruction system.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2014· JK Products & Services, Inc

Recalled Item: SUN DASH RADIUS 252 PN 8000809705. The device is intended Recalled by JK...

The Issue: The integrity of the wires inside main electrical chord become compromised...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2014· Estill Medical Technologies, Inc

Recalled Item: Ultra Battery 1 Model: TA-UB1 NSN: 6515-01-592-5803 The Ultra Battery...

The Issue: Estill has discovered that a fully discharged Ultra Battery 1 (TA-UB1) will...

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

Class II — Potential Health HazardOngoing
DrugJuly 25, 2014· Sandoz Incorporated

Recalled Item: Alprazolam Tablets Recalled by Sandoz Incorporated Due to Presence of...

The Issue: Presence of Foreign Substance; tablets may contain stainless steel metal...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2014· Fagron, Inc

Recalled Item: Fagron Recalled by Fagron, Inc Due to Microbial Contamination of Non-Sterile...

The Issue: Microbial Contamination of Non-Sterile Products: Fagron is recalling six...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2014· Wockhardt Usa Inc.

Recalled Item: Wockhardt Metoprolol Succinate Extended-Release Tablets Recalled by...

The Issue: Failed Dissolution Specifications: Dissolution failures found during testing...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2014· Fagron, Inc

Recalled Item: Fagron Recalled by Fagron, Inc Due to Microbial Contamination of Non-Sterile...

The Issue: Microbial Contamination of Non-Sterile Products: Fagron is recalling six...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2014· Fagron, Inc

Recalled Item: Fagron Recalled by Fagron, Inc Due to Microbial Contamination of Non-Sterile...

The Issue: Microbial Contamination of Non-Sterile Products: Fagron is recalling six...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 24, 2014· GoMacro, Inc.

Recalled Item: gomacro MACROBAR brand almond butter + carob. Net Wt. 2 oz (57 g) Recalled...

The Issue: GoMacro is recalling MARCO BARS brand almond butter + carob (lots 1634 and...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 24, 2014· GoMacro, Inc.

Recalled Item: gomacro MACROBAR brand sunflower butter + chocolate Net Wt. 2.3 oz (65 g)...

The Issue: GoMacro is recalling MARCO BARS brand almond butter + carob (lots 1634 and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 24, 2014· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker T2 Tibia System Nail Insertion Sleeve Recalled by Stryker Howmedica...

The Issue: Stryker Orthopaedics received a report indicating some of the Nail Insertion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Becton Dickinson & Co.

Recalled Item: The BD MAX MRSA Assay Recalled by Becton Dickinson & Co. Due to The...

The Issue: The performance of the assay no longer conforms to this statement in the...

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

Class II — Potential Health HazardOngoing