Product Recalls in Kentucky

Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,542 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,542 in last 12 months

Showing 1696116980 of 28,748 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: VERSYS 7.5 IN BEADED FC +10 CALCAR 13.5X180MM STR +10 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 15X160MM STD BODY STD NECK Prosthesis Recalled by...

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 8 INCH BEADED FC 12X200MM STR STD BODY/NECK 13X200MM Recalled by...

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: LPS-FLEX PRECOAT FEMORAL B-R LPS-FLEX PRECOAT FEMORAL C-L LPS-FLEX PRECOAT...

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 PRECOAT FEM COMP SIZE BMR CR PRECOAT FEM COMP 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: BIPOLAR METAL SHELL 48 MM OD Use of the MultiPolar 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: FEM PRC LT M/RT L SML FEM PRC RT M/LT 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-FLEX GSF OPT SZ C-L¿ LPS-FLEX GSF OPT SZ C-R¿ 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: CR-FLEX POR HATCP FEM C-L CR-FLEX POR HATCP FEM C-R 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-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION...

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 OPTION FEM COMP SIZE C/L CR OPTION FEM COMP 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: LPS PRECOAT FEM SIZE D-RT LPS PRECOAT FEM SIZE E-RT 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 13X160MM LM BODY EXT NECK & STD NECK Prosthesis...

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 0 STD 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· Smiths Medical ASD Inc.

Recalled Item: BCI Advisor Vital Signs Monitor Recalled by Smiths Medical ASD Inc. Due to...

The Issue: Some printing modes on the devices may not function properly (tabular data...

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 STEM 12X160MM LM 13X160MM LM 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: GENDER SOLUTIONS NATURAL-KNEE FLEX SYSTEM GENDER SOLUTIONS FEMALE (GSF)...

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 1 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