Product Recalls in North Dakota

Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,804 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,804 in last 12 months

Showing 2654126560 of 47,938 recalls

DrugNovember 29, 2017· Prinston Pharmaceutical Inc

Recalled Item: Valsartan Tablets Recalled by Prinston Pharmaceutical Inc Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: confirmed customer complaint of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
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: 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 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: 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: 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: CR POR FEM HATCP SIZE E/L SIZE F/L Knee Prosthesis 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 OPT FEM C-L CR-FLEX OPT FEM C-R CR-FLEX OPT 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 7.5 INCH BEADED FC REV 13.5X190MM STRAIGHT 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: LCCK FEM IMPLANT SZ C-L LCCK FEM IMPLANT 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: 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: 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: 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: NEXGEN LPS-FLEX PRECOAT FEMORAL SIZE E-LT This device is indicated 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: ZIMMER PATELLA FEMORAL JOINT¿ Osteoarthritis Recalled by Zimmer Biomet, Inc....

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 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: LPS PRECOAT SRF HDN FEM SZ D-L LPS PRECOAT SRF 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: 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: NEXGEN GSF POROUS FEMORAL LPS FLEX SIZE F Recalled by Zimmer Biomet, Inc....

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