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. 2,375 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,375 in last 12 months

Showing 2470124720 of 27,512 recalls

Medical DeviceAugust 30, 2013· Zimmer, Inc.

Recalled Item: Gender Solutions" Patello-Femoral Component Recalled by Zimmer, Inc. Due to...

The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT Big Bore Oncology Recalled by Philips Medical Systems...

The Issue: There are artifacts appearing on the Tracker images during...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Implantech Associates Inc

Recalled Item: Device Name: Terino Square Chin-Style II-Medium Recalled by Implantech...

The Issue: Implantech initiated a voluntary recall of certain lots of Terino Square...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Zimmer, Inc.

Recalled Item: NexGen¿ Femoral Component (CR-FLEX GSF POR FEM Recalled by Zimmer, Inc. Due...

The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Emit 2000 Phenobarbital Assay and Syva Emit 2000 Phenobarbital Assay...

The Issue: Imprecision with certain lots

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek FMS Outflow Tubing with One-Way valve Product Code:284649...

The Issue: Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Carestream Health Inc.

Recalled Item: CARESTREAM DRX -Mobile Retrofit Kit Recalled by Carestream Health Inc. Due...

The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Vital Diagnostics, Inc.

Recalled Item: Consult Diagnostics¿ Eon Calcium Reagent For In-Vitro Diagnostic Use PN:...

The Issue: High positive calcium bias on plasma sample versus results on serum

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Combiset Blood Line with BVM for Hemodialysis use Catalog Number: Recalled...

The Issue: Updated Instructions for Use: Bloodline connections not tightened per...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Boston Scientific CRM Corp

Recalled Item: Boston Scientific COGNIS CRT-D Recalled by Boston Scientific CRM Corp Due to...

The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Carestream Health Inc.

Recalled Item: DRX- Revolution Recalled by Carestream Health Inc. Due to Carestream Health...

The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek FMS Intermediary Tubing with One-Way valve Product Code:...

The Issue: Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008K@ Home Blood lines Combiset True Flow Series for Hemodialysis Recalled...

The Issue: Updated Instructions for Use: Bloodline connections not tightened per...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Boston Scientific CRM Corp

Recalled Item: Boston Scientific TELIGEN Recalled by Boston Scientific CRM Corp Due to The...

The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Carestream Health Inc.

Recalled Item: Carestream DRX-Revolution Mobile X-Ray System -- Made in U.S.A. by Recalled...

The Issue: It was discovered that Carestream received a report from a customer that 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Steris Corporation

Recalled Item: Reliance Endoscope Processing System (REPS) Recalled by Steris Corporation...

The Issue: The air pipe that delivers unfiltered ambient air from the procedure room...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Combiset Blood Line Hemodialysis use Catalog Number: 03-2622-3. Intended for...

The Issue: Updated Instructions for Use: Bloodline connections not tightened per...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Vital Diagnostics, Inc.

Recalled Item: Vital Diagnostics Envoy Calcium Reagent For In-Vitro Diagnostic Use. PN...

The Issue: High positive calcium bias on plasma sample versus results on serum

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Hospira Inc.

Recalled Item: *** 1) SYMBIQ One-Channel Infuser Recalled by Hospira Inc. Due to Hospira...

The Issue: Hospira shipped the incorrect replaceable battery pack (Part No:...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Carefusion 2200 Inc

Recalled Item: *** 1) Cat. 4341B Recalled by Carefusion 2200 Inc Due to Catheters included...

The Issue: Catheters included in Thoracentesis Tray and Safe-T Thoracentesis Tray -...

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

Class II — Potential Health HazardOngoing