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. 2,529 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,529 in last 12 months

Showing 1054110560 of 47,938 recalls

Medical DeviceNovember 8, 2022· Companion Medical, Inc.

Recalled Item: InPen Diabetes Management App Recalled by Companion Medical, Inc. Due to...

The Issue: Diabetes management app may crash immediately upon opening, while using the...

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

Class II — Potential Health HazardOngoing
FoodNovember 7, 2022· Betty Buzz LLC

Recalled Item: Betty Buzz Sparkling Grapefruit - Non-alcoholic Beverage & Mixer Container...

The Issue: Beverage has off-odor

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 7, 2022· R & D Systems, Inc.

Recalled Item: R&D CBC-3D Hematology Control: (1) CBC-3D Normal Pack Hematology Control...

The Issue: For one lot of CBC-3D Hematology Control, the Normal Level may exhibit...

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

Class III — Low RiskOngoing
Medical DeviceNovember 7, 2022· Cordis US Corp

Recalled Item: Cordis Angiographic Catheter Extensions. Used to transport fluid from the...

The Issue: There is a potential for separation at the male connector.

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

Class II — Potential Health HazardOngoing
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
DrugNovember 5, 2022· Adam's Polishes LLC

Recalled Item: Adam's Polishes ALCOHOL BASED HAND SANITIZER Recalled by Adam's Polishes LLC...

The Issue: CGMP Deviations: Other lots of hand sanitizer are being recalled because...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 5, 2022· Adam's Polishes LLC

Recalled Item: Adam's Polishes ALCOHOL BASED HAND SANITIZER Recalled by Adam's Polishes LLC...

The Issue: Chemical Contamination: FDA analysis found 1 lot of Adam's Polishes ALCOHOL...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
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
FoodNovember 3, 2022· Nestle-USA, Inc. (Corporate Office)

Recalled Item: Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in Recalled by...

The Issue: Potential of foreign material within product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
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