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. 2,535 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,535 in last 12 months

Showing 89218940 of 27,512 recalls

Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge with software syngo.CT VB20 Model #10590000 Recalled...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force with software syngo.CT VB20 Model #10742326 Recalled by...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash with software syngo.CT VB20 Model #10430603...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2021· PTW NORTH AMERICA CORPORATION

Recalled Item: Software BeamAdjust version 2.2 Recalled by PTW NORTH AMERICA CORPORATION...

The Issue: When a measurement with a PTW detector array is performed with the software...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2021· North Coast Medical Inc

Recalled Item: Norco Ultrasound Gel Recalled by North Coast Medical Inc Due to Ultrasound...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 27, 2021· North Coast Medical Inc

Recalled Item: EcoLotion Transmission Lotion Recalled by North Coast Medical Inc Due to...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 27, 2021· Uoc Usa Inc

Recalled Item: United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part...

The Issue: Due to product not meeting specification for concentricity and failing to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· Atrium Medical Corporation

Recalled Item: Atrium Pneumostat Chest Drain Valve Recalled by Atrium Medical Corporation...

The Issue: The firm is revising the Indication for Use, Contraindications, Warnings,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Instrumentation Laboratory

Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...

The Issue: Labeled On-board instrument stability issue for current and future lots,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Deerfield Imaging, Inc.

Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...

The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Instrumentation Laboratory

Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...

The Issue: Labeled On-board instrument stability issue for current and future lots,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Atrium Medical Corporation

Recalled Item: Atrium ADVANTA VXT Vascular Graft Recalled by Atrium Medical Corporation Due...

The Issue: The product package may potentially contain a mismatched graft that does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Accelerated Care Plus Corporation

Recalled Item: Omnisound Gel Recalled by Accelerated Care Plus Corporation Due to...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 25, 2021· Deerfield Imaging, Inc.

Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...

The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Deerfield Imaging, Inc.

Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...

The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Instrumentation Laboratory

Recalled Item: HemosIL Liquid Anti-Xa- automated chromogenic assay for in vitro diagnostic...

The Issue: Labeled On-board instrument stability issue for current and future lots,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheters Recalled by Medtronic Perfusion Systems Due to...

The Issue: Potential for a wire protrusion through the left heart vent catheter tip

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder...

The Issue: Potential for difficulty in safety mechanism activation.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· National Distribution & Contracting Inc

Recalled Item: ECO 85CB Lotion Ultrasound 8.5 oz 24/cs ECO 40JBC Gel Recalled by National...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder...

The Issue: Potential for difficulty in safety mechanism activation.

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

Class II — Potential Health HazardOngoing