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. 1,032 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,032 in last 12 months

Showing 14661–14680 of 47,938 recalls

Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Ingenia 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T Evoluton- Magnetic Resonance Medical Electrical Systems...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Ingenia CX 3.0T-Magnetic Resonance Medical Electrical Systems indicated for...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Paragon 28, Inc.

Recalled Item: Phantom Nail System Recalled by Paragon 28, Inc. Due to A thin wall...

The Issue: A thin wall condition between the inner cannulation and the flutes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Getinge Dominican Republic SA

Recalled Item: Arjo Disposable Repositioning Sling Recalled by Getinge Dominican Republic...

The Issue: Sling loop straps on device pose a trip hazard.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T-Magnetic Resonance Medical Electrical Systems indicated for use...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Ingenia Elition S-Magnetic Resonance Medical Electrical Systems indicated...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Achieva 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Ingenia Elition X-Magnetic Resonance Medical Electrical Systems indicated...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

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

Class II — Potential Health HazardOngoing
DrugJuly 30, 2021· Custopharm, Inc.

Recalled Item: FLUDARABINE PHOSPHATE FOR INJECTION Recalled by Custopharm, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility: the manufacturing firm had microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2021· Noven Pharmaceuticals Inc

Recalled Item: Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.25 mg...

The Issue: Failed Stability Specifications; out of specification for shear.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2021· Noven Pharmaceuticals Inc

Recalled Item: Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.14 mg...

The Issue: Failed Stability Specifications; out of specification for shear.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Adenosine Injection Recalled by Teva Pharmaceuticals USA Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Leucovorin Calcium for Injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Vecuronium Bromide for Injection 10 mg Recalled by Teva Pharmaceuticals USA...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Octreotide Acetate Injection 1000 mcg/5mL Recalled by Teva Pharmaceuticals...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Methylprednisolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Idarubicin Hydrochloride Injection 20 mg/20 mL Recalled by Teva...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Octreotide Acetate Injection 100 mcg/mL Recalled by Teva Pharmaceuticals USA...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Octreotide Acetate Injection 50 mcg/mL Recalled by Teva Pharmaceuticals USA...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund