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. 2,582 recalls have been distributed to Hawaii in the last 12 months.
Showing 1801–1820 of 27,645 recalls
Recalled Item: Guide Wire with Ruler Tube 3x800 mm DIA Recalled by Stryker GmbH Due to The...
The Issue: The metal ring at the end of the Guide Wire with Ruler Tube may detach from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guide Wire with Ruler Tube 3x1000 mm DIA Recalled by Stryker GmbH Due to The...
The Issue: The metal ring at the end of the Guide Wire with Ruler Tube may detach from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GALT Guidewire Guidewires are intended for use in Recalled by Galt Medical...
The Issue: Due to a potential open seal in the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B Braun Interventional Coaxial Dilator Recalled by Galt Medical Corporation...
The Issue: Due to a potential open seal in the sterile barrier packaging .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B Braun Interventional ELITE HV Hemostasis Valve Introducer System by Galt...
The Issue: Due to a potential open seal in the sterile barrier packaging .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraocular Lens. enVista Envy IOL Recalled by Bausch & Lomb Surgical, Inc....
The Issue: In response to an increased number of reports of toxic anterior segment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Introducer Kit- Tearaway MicroSlide Recalled by Galt Medical Corporation Due...
The Issue: Due to a potential open seal in the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Introducer Needle These needles are used for the Recalled by Galt Medical...
The Issue: Due to a potential open seal in the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Introducer Kit- Coaxial Dilator Recalled by Galt Medical Corporation Due to...
The Issue: Due to a potential open seal in the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraocular lens. enVista Monofocal IOL Recalled by Bausch & Lomb Surgical,...
The Issue: In response to an increased number of reports of toxic anterior segment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GALT Centeze Catheter DRC-002-06 The Centeze is intended Recalled by Galt...
The Issue: Due to a potential open seal in the sterile barrier packaging .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount Recalled by IHB OPERATIONS...
The Issue: The mounting hardware that is supplied with the 4FXS-60 monitor bracket does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: restor3d Cordera Hip System. ACETABULAR LINER GRP C 36MM LIP. Recalled by...
The Issue: The hip cup liner that was packaged with the incorrect labeling....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Explorer/Nova Dual Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Master/Nova Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 3.0T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.0T Omni/Stellar Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enterprise 1.5T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Omni/Stellar Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.