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. 2,475 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,475 in last 12 months

Showing 1644116460 of 27,645 recalls

Medical DeviceNovember 29, 2017· Zimmer Dental Inc

Recalled Item: Tapered Screw-Vent MTX Recalled by Zimmer Dental Inc Due to Mislabeling

The Issue: Two lots of the Tapered Screw-Vent Implants, with different outer thread...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: CR-FLEX POR FEM F-L CR-FLEX POR FEM F-R MINUS CR-FLEX Recalled by Zimmer...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: VERSYS 6 INCH BEADED FC 14X160MM STD BODY EXT & STD NECK Prosthesis Recalled...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: LPS OPTION FEMORAL C-L LPS OPTION FEMORAL C-R LPS OPTION Recalled by Zimmer...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: CR-FLX POR HATCP FEM C-L MINUS CR-FLX POR HATCP FEM Recalled by Zimmer...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: LPS FEM IMPLANT SZ H-R This device is indicated for Recalled by Zimmer...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: CPT 12/14 COCR SIZE 2 EXT prosthesis Recalled by Zimmer Biomet, Inc. Due to...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: LPS POROUS FEM IMPLANT SZ G-L LPS PRECOAT FEM IMPLANT Recalled by Zimmer...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: CR-FLEX PCT FEM C-R MINUS CR-FLEX PCT FEM D-L MINUS Recalled by Zimmer...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: CPT 12/14 COCR REVISION SIZE 2 180MM prosthesis Recalled by Zimmer Biomet,...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Dental Inc

Recalled Item: Tapered Screw-Vent MTX Recalled by Zimmer Dental Inc Due to Mislabeling

The Issue: Two lots of the Tapered Screw-Vent Implants, with different outer thread...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: PATELLO-FEMORAL JOINT SYSTEM GENDER SOLUTIONS PATELLO-FEMORAL¿...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: VERSYS 6 INCH BEADED FC 12X160MM LM BODY EXT NECK Recalled by Zimmer Biomet,...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Partial Knee spacer block instruments Recalled by Zimmer Biomet,...

The Issue: Certain partial knee implant spacer blocks do not fit in the alignment tower...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: CR-FLEX GSF PCT SZ C-R MINUS¿ CR-FLEX GSF PCT SZ Recalled by Zimmer Biomet,...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: GENDER SOLUTIONS NATURAL-KNEE FLEX SYSTEM FEMORAL COMPONENT¿ N-K FLX GSM...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Cincinnati Sub-Zero Products LLC

Recalled Item: Hemotherm¿ Dual Reservoir Cooler/Heater System Models 400CE and 400MR...

The Issue: Due to FDA's safety communication relating to nontuberculous mycobacteria...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Ethicon, Inc.

Recalled Item: DERMABOND" PRINEO" Skin Closure System Product Usage: DERMABOND PRINEO...

The Issue: Ethicon discovered that specific lots of DERMABOND"PRINEO"System may not dry...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Syva¿ EMIT¿ 2000 Theophylline Product Usage: The Syva¿ Emit¿ 2000 Recalled...

The Issue: Lot J1 of the Syva¿ EMIT¿ 2000 Theophylline Assay, when run on a Beckman AU...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2017· SANTA JOY ORNAMENT & GIFTWARE CO

Recalled Item: Santajoy Ornament & Giftware Co. Recalled by SANTA JOY ORNAMENT & GIFTWARE...

The Issue: It was discovered that the product units it imported may, at peak levels,...

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

Class II — Potential Health HazardOngoing