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. 1,739 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,739 in last 12 months

Showing 3798138000 of 47,938 recalls

FoodFebruary 6, 2015· MegaMex Foods, LLC - R&D Center

Recalled Item: Herdez Chilpotle Peppers Recalled by MegaMex Foods, LLC - R&D Center Due to...

The Issue: MegaMex Foods is recalling Herdez Chilpotle Peppers product due to an...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 6, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS SOMATOM Force with software version VA50A and /or VA50A_FP1 Recalled...

The Issue: Possibility of image artifacts during data acquisition when using Adaptive...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2015· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo HX2 Temperature Management System provides temperature control of two...

The Issue: Malfunctioning mixing valve and loss of cooling and/or heating capability....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Derma Pen, LLC

Recalled Item: DermaPen Pro Model Recalled by Derma Pen, LLC Due to Derma Pen initiated a...

The Issue: Derma Pen initiated a field communication for Dermapen after receiving an...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Brilliance CT 64-channel with Essence...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray systems Brilliance iCT Recalled by Philips Medical...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Ingenuity CT scanners. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Ingenuity Core. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Brilliance iCT SP. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Ingenuity Core 128. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems (Brilliance CT 64-channel w/Essence...

The Issue: Philips discovered that a software defect exists in marketed product wherein...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Zipline Medical

Recalled Item: Zip 8i Surgical Skin Closure Device Recalled by Zipline Medical Due to The...

The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Remel Inc

Recalled Item: Oxoid Legionella BCYE Growth Supplement SR0110A packaged in packs of...

The Issue: Use of the product may not provide adequate recovery and could result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Arrow International Inc

Recalled Item: ARROW FiberOptix Intra-Aortic Balloon Catheter Kit Recalled by Arrow...

The Issue: Outer package product label incorrectly identifies the product as FiberOptix...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Zipline Medical

Recalled Item: Zip 8M Wound Closure Device Recalled by Zipline Medical Due to The...

The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Zipline Medical

Recalled Item: Zip 16 Surgical Skin Closure Device Recalled by Zipline Medical Due to The...

The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...

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

Class II — Potential Health HazardOngoing
FoodFebruary 4, 2015· Health One Pharmaceuticals Inc

Recalled Item: Femanol Recalled by Health One Pharmaceuticals Inc Due to Health One...

The Issue: Health One Pharmaceuticals is recalling dietary supplements due to...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 4, 2015· Health One Pharmaceuticals Inc

Recalled Item: Bone Rebuilder Recalled by Health One Pharmaceuticals Inc Due to Health One...

The Issue: Health One Pharmaceuticals is recalling dietary supplements due to...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 4, 2015· Health One Pharmaceuticals Inc

Recalled Item: SOD Recalled by Health One Pharmaceuticals Inc Due to Health One...

The Issue: Health One Pharmaceuticals is recalling dietary supplements due to...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 4, 2015· Health One Pharmaceuticals Inc

Recalled Item: EST -700 Calcium Recalled by Health One Pharmaceuticals Inc Due to Health...

The Issue: Health One Pharmaceuticals is recalling dietary supplements due to...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund