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. 2,480 recalls have been distributed to Hawaii in the last 12 months.
Showing 14721–14740 of 27,645 recalls
Recalled Item: BD Max Instrument Recalled by Becton Dickinson & Co. Due to A trend for...
The Issue: A trend for false positive Candida glabrata results has been confirmed. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Max Instrument Reader Spare Part Recalled by Becton Dickinson & Co. Due...
The Issue: A trend for false positive Candida glabrata results has been confirmed. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FocalPoint Slide Profiler and BD FocalPoint GS Review Station Recalled by...
The Issue: The device may not function at the lower end (<15 deg. C) of the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit Recalled by Arrow International Inc Due to...
The Issue: The products labeling contains inconsistencies. In certain instances, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4.5 Recalled by RAYSEARCH LABORATORIES AB Due to Robust...
The Issue: Robust optimization for plans using beam set + background dose is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD) Recalled by DePuy...
The Issue: There is the potential for debris/material to be found behind the O-rings in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORAIL AMT HIGH OFFSET NECK SEGMENT (KHO) Recalled by DePuy Orthopaedics,...
The Issue: There is the potential for debris/material to be found behind the O-rings in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORAIL AMT COXA VARA NECK SEGMENT (KLA) Pro. Code L20432 Recalled by DePuy...
The Issue: There is the potential for debris/material to be found behind the O-rings in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StageOne Hip Recalled by Zimmer Biomet, Inc. Due to There is a potential for...
The Issue: There is a potential for comingling of the 43MM and 51 MM molds
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...
The Issue: Potential for leaking product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...
The Issue: Potential for leaking product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...
The Issue: Potential for leaking product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExactaMix Recalled by The Metrix Company Due to Potential for leaking product
The Issue: Potential for leaking product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...
The Issue: Potential for leaking product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExactaMix Recalled by The Metrix Company Due to Potential for leaking product
The Issue: Potential for leaking product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...
The Issue: Potential for leaking product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...
The Issue: Potential for leaking product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AS-OBGYN Information System version 7.824.x Recalled by AS Software, Inc....
The Issue: Any change made to current ultrasound machine software or hardware upgrades,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single-Use Biopsy Forceps Recalled by Micro-Tech (Nanjing) Co., Ltd. Due to...
The Issue: Single-Use Biopsy Forceps box contains incorrect product, instead it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid IABP Recalled by Maquet Datascope Corp - Cardiac Assist...
The Issue: There is a potential for interruption and/or inability to start therapy to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.