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. 1,061 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,061 in last 12 months

Showing 7881–7900 of 27,512 recalls

Medical DeviceJune 1, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte 2301 2K 3.0 Ca 1 Mg Gal Recalled by Fresenius Medical Care...

The Issue: The product was potentially exposed to below-recommended storage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2022· Ultradent Products, Inc.

Recalled Item: Peak Universal Bond Self-Etch Bottle Kit Recalled by Ultradent Products,...

The Issue: SE primer may be missing some or all of the resin portion of the chemistry....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2022· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 9B SP1. For radiation treatment planning. Recalled by RAYSEARCH...

The Issue: An issue with propagation of treatment course information from RayStation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2022· Baxter Healthcare Corporation

Recalled Item: NaviCare Nurse Call/Voalte Nurse Call Recalled by Baxter Healthcare...

The Issue: An issue has been identified with Phillips (Emergin) and Longleaf non relay...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2022· Spacelabs Healthcare, Inc.

Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...

The Issue: Software related alarm escalation defect occurs after approximately 25 days...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2022· Ossur Americas

Recalled Item: OSSUR VARIFLEX SUBA JUNIOR foot and ankle external prosthesis Recalled by...

The Issue: Due to receiving complaints related to broken (cracked) prosthetic foot with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2022· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Anti-SARS-CoV-2 IgG Quantitative Reagent Pack- Intended for use on VITROS¿...

The Issue: On-Analyzer Stability (OAS) time, supported for 6 weeks; not 8 weeks as is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2022· Olympus Corporation of the Americas

Recalled Item: SOLTIVE SuperPulsed Laser Fibers Recalled by Olympus Corporation of the...

The Issue: Device model and size for affected lots of Laser Fibers may be mismatched...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2022· Paragon 28, Inc.

Recalled Item: HammerTube Implant Recalled by Paragon 28, Inc. Due to Due to Titanium...

The Issue: Due to Titanium plasma coating not present implant.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: 3M COMPANY 3M PAD Recalled by Mckesson Medical-Surgical Inc. Corporate...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Fischer Cone Biopsy Excisor EXCISOR Recalled by Mckesson Medical-Surgical...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: BEAVER-VISITEC INTERNATIONAL Recalled by Mckesson Medical-Surgical Inc....

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: a. METREX RESEARCH CORP CaviCide1 DISINFECTANT Recalled by Mckesson...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: MEDLINE INDUSTRIES Medline Catheter Insertion Tray Medline Foley Without...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Mckesson GYNECATH H/S CATHETER 5FR (10/CS) Model Number: 11-19610 Recalled...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: COOPER SURGICAL Milex PESSARY Recalled by Mckesson Medical-Surgical Inc....

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: MERIT MEDICAL SYSTEMS Temno Soft Tissue Biopsy Device Temno 14 Recalled by...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Cook Incorporated

Recalled Item: Pressure Monitoring Set Recalled by Cook Incorporated Due to The products...

The Issue: The products may contain excess coating material on the outside and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: SPS MEDICAL SUPPLY Crosstex International Sterilization Roll Sani-Roll...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class III — Low RiskOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: a. Alcon Clear Care Contact Lens Solution Clear Care 12 oz. Solution...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing