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. 1,047 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
1,047 in last 12 months

Showing 15381–15400 of 47,764 recalls

Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL494...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NO156Z...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL470...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· GE Healthcare, LLC

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

The Issue: GE Healthcare has become aware of a potential issue on the Revolution CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer - Product Usage: intended to assist in the...

The Issue: When the Cross Enterprise Display option is enabled on the Centricity...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Interventional Fluoroscopic X-Ray System ARTIS icono biplane- 11327600 ARTIS...

The Issue: Siemens has become aware of a potential issue with software version VE20C....

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

Class II — Potential Health HazardOngoing
DrugMarch 19, 2021· X-Gen Pharmaceuticals Inc.

Recalled Item: Neomycin Sulfate Tablets Recalled by X-Gen Pharmaceuticals Inc. Due to...

The Issue: Failed Stability Specifications: Out of Specification (OOS) result reported...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: ChloraPrep With Tint 2% w/v chlorhexidine gluconate (CHG) and 70% Recalled...

The Issue: CGMP Deviations: Product is being recalled because at labeled storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Clear Recalled by CareFusion 213, LLC Due to...

The Issue: Non-sterility.Product is being recalled because at labeled storage...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: ChloraPrep One-Step 2% w/v chlorhexidine gluconate (CHG) and 70% v/v...

The Issue: Microbial Contamination of Non-Sterile Product.Product is being recalled...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Hi-Lite Orange 2% w/v chlorhexidine gluconate (CHG) and...

The Issue: Non-sterility.Product is being recalled because at labeled storage...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Hi-Lite Orange 2% w/v chlorhexidine gluconate (CHG) and...

The Issue: Lack of Assurance of Sterility: Product is being recalled because at labeled...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Clear Recalled by CareFusion 213, LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Product is being recalled because at labeled...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: ChloraPrep With Tint 2% w/v chlorhexidine gluconate (CHG) and 70% Recalled...

The Issue: Microbial Contamination of Non-Sterile Product:.Product is being recalled...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: ChloraPrep One-Step 2% w/v chlorhexidine gluconate (CHG) and 70% v/v...

The Issue: CGMP Deviations: Product is being recalled because at labeled storage...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 18, 2021· Coltene Whaledent Inc

Recalled Item: Dental pins - TMS LINK PLUS Self-Threading Pins - Product Recalled by...

The Issue: The incorrect dental pins were packaged and subsequently distributed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2021· Luminex Corporation

Recalled Item: VERIGENE Processor SP - Product Usage: intended for processing and Recalled...

The Issue: Potential for a false-negative result for Vibrio parahaemolyticus,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: AquaBplus and AquaBplus B2 Water Purification System - Product Usage:...

The Issue: AquaBplus HF module on the AquaBplus 2500 osmosis system, an error in the US...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2021· Gentueri Inc

Recalled Item: Gentueri Viral Transport Medium (VTM) Recalled by Gentueri Inc Due to Medium...

The Issue: Medium showed visual turbidity and discoloration, potentially contaminating...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Becton Dickinson & Co.

Recalled Item: BD BBL Martin-Lewis Agar Recalled by Becton Dickinson & Co. Due to Products...

The Issue: Products show heavy growth of C. albicans after 24 hours of incubation due...

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

Class II — Potential Health HazardOngoing