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. 2,412 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,412 in last 12 months

Showing 2060120620 of 27,645 recalls

Medical DeviceNovember 30, 2015· Verathon, Inc.

Recalled Item: GlideScope Video Laryngoscope (GVL) Recalled by Verathon, Inc. Due to...

The Issue: Certain models and serial numbers of GlideScope GVL and AVL laryngoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Verathon, Inc.

Recalled Item: GlideScope AVL Video Laryngoscope (AVL) Recalled by Verathon, Inc. Due to...

The Issue: Certain models and serial numbers of GlideScope GVL and AVL laryngoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Acumedia Manufacturers, Inc.

Recalled Item: Palcam Supplement Acumedia PN 7987 Product Usage: PALCAM Supplement is...

The Issue: Contamination of product with possible Bacillus spp

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2015· Leica Microsystems, Inc.

Recalled Item: Bond Polymer Red Detection DS9390 kits. The common name Recalled by Leica...

The Issue: The Firm informed the importer/distributor, Leica Microsystems, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Preformance Post Dental implants Recalled by Biomet 3i, LLC Due to...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Abeon Medical Corporation

Recalled Item: TLC¿ Self-Retaining Retractor Frames SINGLE USE ONLY Rx ONLY (USA) Recalled...

The Issue: The firm was notified by some of their customers that some of the sealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Titanium Square Uniscrew Dental implants Recalled by Biomet 3i, LLC Due to...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: IOL Transfer Impression Coping Dental implants Recalled by Biomet 3i, LLC...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Gingihue 15 Degree Pre-Angled Post Dental implants Recalled by Biomet 3i,...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Gingihue Post Dental implants Recalled by Biomet 3i, LLC Due to Pouches may...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Titanium Hexed Uniscrew Dental implants Recalled by Biomet 3i, LLC Due to...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain EP Twist Lock TM Coping Dental implants Recalled by Biomet 3i, LLC...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Gingihue Post 3.4mm(D) x 3.8mm(P) x 2mm(H) Item: IMAP32G Recalled by...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: IOL Titanium Temporary Cylinder Dental implants Recalled by Biomet 3i, LLC...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Preformance Temporary Cylinder Dental implants Recalled by Biomet...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Preformance Post Dental implants Recalled by Biomet 3i, LLC Due to Pouches...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Conical Abutment Dental implants Recalled by Biomet 3i, LLC Due to Pouches...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Locator Light Retention Replacement Males 4pk Dental implants Recalled by...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Conical Abutment Gold Standard ZR TM Dental implants Recalled by Biomet 3i,...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Gold Slotted Screw Dental implants Recalled by Biomet 3i, LLC Due to Pouches...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing