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. 2,573 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,573 in last 12 months

Showing 24412460 of 27,512 recalls

Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE Recalled...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: ECONO STERILE SIMS Recalled...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE brand medical procedure kits labeled as: 1) ECONO Recalled by...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: ECONO STERILE SCHAMBERG...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: ECONO STERILE IRIS Recalled...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: ECONO STERILE BLAKE...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE Recalled...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE Recalled...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: ECONO STERILE CEMENT...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: ECONO STERILE IUD Recalled...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· Coloplast Manufacturing US, LLC

Recalled Item: X-Flow prostatectomy catheter Recalled by Coloplast Manufacturing US, LLC...

The Issue: A possible sterility issue was detected in Coloplast's facility on some...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· A L I Technologies Ltd

Recalled Item: Change Healthcare Cardiology Hemo software Recalled by A L I Technologies...

The Issue: Software defect concerning autosave mechanism may result in the clinician...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· Accriva Diagnostics, Inc.

Recalled Item: VerifyNow P2Y12 Platelet Reactivity Test Recalled by Accriva Diagnostics,...

The Issue: Platelet Reactivity Test distributed without appropriate US-FDA market...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· A L I Technologies Ltd

Recalled Item: McKesson Cardiology Hemo software Recalled by A L I Technologies Ltd Due to...

The Issue: Software defect concerning autosave mechanism may result in the clinician...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· A L I Technologies Ltd

Recalled Item: Change Healthcare Cardiology Hemodynamics software Recalled by A L I...

The Issue: Software defect concerning autosave mechanism may result in the clinician...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· Coloplast Manufacturing US, LLC

Recalled Item: Folysil Silicone Foley Catheters Recalled by Coloplast Manufacturing US, LLC...

The Issue: A possible sterility issue was detected in Coloplast's facility on some...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· Moximed, Inc.

Recalled Item: MISHA Knee System Implant Small Recalled by Moximed, Inc. Due to Knee...

The Issue: Knee implant may fracture due to a supplier-related issue with one component...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2024· IsoTis OrthoBiologics, Inc.

Recalled Item: OsteoSurge 100 Demineralized Bone Matrix Putty with Accell Bone Matrix...

The Issue: Incorrect expiration date listed on the outer box, which does not align with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2024· IsoTis OrthoBiologics, Inc.

Recalled Item: OsteoCove Putty Recalled by IsoTis OrthoBiologics, Inc. Due to Hydration...

The Issue: Hydration issue resulting in the product being less cohesive and moldable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2024· O&M HALYARD, INC.

Recalled Item: Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number:...

The Issue: Elevated residues of anti-block/slip additive used in manufacturing found...

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

Class II — Potential Health HazardOngoing