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. 2,557 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,557 in last 12 months

Showing 37213740 of 27,512 recalls

Medical DeviceMay 31, 2024· Olympus Corporation of the Americas

Recalled Item: Soltive Pro SuperPulsed Laser System Recalled by Olympus Corporation of the...

The Issue: Difficulties in pairing the wireless footswitch with the Soltive Laser,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Olympus Corporation of the Americas

Recalled Item: Soltive SuperPulsed Laser System Wireless Footswitch Recalled by Olympus...

The Issue: Difficulties in pairing the wireless footswitch with the Soltive Laser,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Radiometer Medical ApS

Recalled Item: ABL800 FLEX Model Numbers 393-800 and 393-801 The ABL800 FLEX Recalled by...

The Issue: Issue with analyzer when the pH of the calibration solution decreases during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Stryker Sustainability Solutions

Recalled Item: Recalled by Stryker Sustainability Solutions Due to Mislabeling

The Issue: Mislabeling; tourniquet cuff packaging labeled as dual port single bladder...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Maquet Cardiovascular, LLC

Recalled Item: The VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems is designed for...

The Issue: There were 27 complaints between March 22, 2024, and April 30, 2024, related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Zoll Medical Corporation

Recalled Item: ZOLL Powerheart G5 AED Recalled by Zoll Medical Corporation Due to G5...

The Issue: G5 Semi-Automatic AED is shipped, with a protective film over its front...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Maquet Cardiovascular, LLC

Recalled Item: The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed...

The Issue: There were 27 complaints between March 22, 2024, and April 30, 2024, related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Vertix MD - The Vertix MD Trauma has been Recalled by Siemens Medical...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: MULTIX TOP - Intended Use: The Multix TOP I PRO Recalled by Siemens Medical...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MP - Inended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: MULTIX TOP - Intended Use: The Multix TOP I PRO Recalled by Siemens Medical...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MP - Intended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Vertix Solitaire - The Vertix MD Trauma has been Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MT - Intended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MT - Intended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: ZE for Vertix Solitaire - The AXIOM Vertix Solitaire is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2024· Baxter Healthcare Corporation

Recalled Item: Volara System. Single Patient Use (SPU) Circuit 5kit for Volara Recalled by...

The Issue: Potential of the handset plug to disconnect from the nebulizer port on the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 30, 2024· Baxter Healthcare Corporation

Recalled Item: Volara System. Blue Ventilator Adapter Module. Intermittent positive...

The Issue: Potential of the handset plug to disconnect from the nebulizer port on the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 30, 2024· Dental EZ Group Star Dental Division

Recalled Item: Titan Scaler Tip - Perio Model/Catalog Number: 261669 The scaler Recalled by...

The Issue: Tip holder portion of the scaler tip assembly may have an oversized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2024· Dental EZ Group Star Dental Division

Recalled Item: Titan Blis-Sonic Scaler packaged with the Titan Scaler Tip - Recalled by...

The Issue: Tip holder portion of the scaler tip assembly may have an oversized...

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

Class II — Potential Health HazardOngoing