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. 2,404 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,404 in last 12 months

Showing 1932119340 of 27,512 recalls

Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T090-000 90" 20 Drop IV Admin Set. Packaged in a Tyvek pouch Recalled by...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-000WF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-022F with 0.22 micron filter and FP Clip. Packaged in a Tyvek pouch...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-120F with 1.2 micron filter and FP Clip. Packaged in a Tyvek pouch...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T090-000W 90" 20 Drop IV Admin Set w/2 Needlefree Y-Sites Recalled by...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-000VF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T030-000 -30" 20 Drop IV Admin Secondary Set. Packaged in a Tyvek pouch...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2016· Cardiovascular Systems Inc

Recalled Item: ViperWire Advance Peripheral Guide Wire Recalled by Cardiovascular Systems...

The Issue: The pouch label was missing the use by date (UBD) of 2018-04.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2016· Dako North America Inc.

Recalled Item: Dako HER2 CISH pharmDx Kit Recalled by Dako North America Inc. Due to An...

The Issue: An incorrect HER2 probe concentration was used when producing the probe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2016· Biomet, Inc.

Recalled Item: TSP Hip Fracture Plating System device Recalled by Biomet, Inc. Due to...

The Issue: The screw may fracture at the junction of the shaft and the head during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2016· Terumo Cardiovascular Systems Corporation

Recalled Item: HX2" Temperature Management Systems Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) is conducting a voluntary recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2016· Terumo Cardiovascular Systems Corporation

Recalled Item: Preamendments device-Sarns Dual Cooler-Heater. The Sarns Dual Cooler-Heater...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) is conducting a voluntary recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Peripherally Inserted Central Catheters (PICC) Recalled by Angiodynamics...

The Issue: There is a potential for stylet stiffening that is not accurately...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2016· Heartware, Inc.

Recalled Item: HeartWare Ventricular Assist System Controller Product Usage: For use as...

The Issue: Loose connector ports in controller body.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Peripherally Inserted Central Catheters (PICC) Recalled by Angiodynamics...

The Issue: There is a potential for stylet stiffening that is not accurately...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2016· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns TCM II Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) is conducting a voluntary recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2016· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns TCM Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) is conducting a voluntary recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2016· Tosoh Bioscience, Inc.

Recalled Item: Instructions for Use (IFU) for Progesterone 3 Calibrator Set Recalled by...

The Issue: Instructions For Use had incorrect lot number and calibrator values

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

Class III — Low RiskOngoing
Medical DeviceJune 7, 2016· Synthes (USA) Products LLC

Recalled Item: Depuy Synthes Trauma- Trochanteric Fixation Nail Advanced (TFNA) Blade/Screw...

The Issue: DePuy Synthes is initiating a voluntary medical device recall due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2016· Stryker Neurovascular

Recalled Item: Target Detachable Coils: TARGET HELICAL NANO 1 MM X 3 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some units of Target Nano...

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

Class II — Potential Health HazardOngoing