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 72417260 of 27,512 recalls

Medical DeviceNovember 7, 2022· Getinge Usa Sales Inc

Recalled Item: Flow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System...

The Issue: The power backup battery, under certain conditions, may exhibit reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2022· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Port a Cath Kit Recalled by Medical Action...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests Japan...

The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests (600T)-...

The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests OUS...

The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2022· Olympus Corporation of the Americas

Recalled Item: HF Resection Electrodes Recalled by Olympus Corporation of the Americas Due...

The Issue: An incompatible HF cable may be packaged with the HF Resection Electrodes....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2022· Icotec Ag

Recalled Item: VADER Pedicle System Torque Wrench Recalled by Icotec Ag Due to During...

The Issue: During internal testing (at manufacturer site) of two torque wrench devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· SynCardia Systems LLC

Recalled Item: SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total...

The Issue: Due to tears reported tears in the cannula due to wear and tear stress.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing