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. 2,553 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,553 in last 12 months

Showing 51615180 of 27,512 recalls

Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ARTERIAL BUNDLE NO CATHETER Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE TRAY TRACH BASIC SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2023· Maquet Medical Systems USA

Recalled Item: CARDIOHELP-i Heart Lung Support System: Blood oxygenation and carbon dioxide...

The Issue: CARDIOHELP-i System was not properly tested to measure leakage current

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

Class III — Low RiskOngoing
Medical DeviceNovember 13, 2023· Randox Laboratories Ltd.

Recalled Item: Calibration Serum Level 3. CAL 3 Recalled by Randox Laboratories Ltd. Due to...

The Issue: There have been transcription errors on the Instructions For Use (IFU) of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2023· Steris Corporation

Recalled Item: Hookup Accessories used with MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS...

The Issue: Identification label on affected hookups could become illegible over time...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2023· Blue Belt Technologies, Inc

Recalled Item: CORI REAL INTELLIGENCE Robotic Drill Recalled by Blue Belt Technologies, Inc...

The Issue: Possibility that the user is unable to resolve drill disconnection error...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2023· Maquet Medical Systems USA

Recalled Item: Venous probe connection cable ( and 701048804) used with Recalled by Maquet...

The Issue: Firm received complaints of breaks in the insulation, shielding, or wires of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: HIGH PRESSURE ROTATOR WITH MALE LUER LOCK Recalled by Smiths Medical Asd Inc...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 6-7-8. indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 16-17-18. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 13.5-14.5-15.5. Indicated for endoscopic...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 6-7-8. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing