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 91019120 of 27,512 recalls

Medical DeviceAugust 4, 2021· Cardinal Health

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...

The Issue: Potential for the plunger to draw back after the air has been expelled and...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 3, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: AquaBplus Water Purification System Recalled by Fresenius Medical Care...

The Issue: AquaBplus HF module on the AquaBplus 2000 osmosis system, an error in the US...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2021· Luminex Corporation

Recalled Item: Verigene EP Amplification Reagent Kit Test Recalled by Luminex Corporation...

The Issue: There is potential for false positive results.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2021· Olympus Corporation of the Americas

Recalled Item: Arc Endocuff Vision as follows: ARV110 ENDOCUFF-V M BLUE PK8 Recalled by...

The Issue: Packaging seal defect may allow a breach of the package sterile barrier and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: uEXPLORER PET/CT System - Product Usage: intended to be operated Recalled by...

The Issue: The EXAM acquisition workflow could occasionally freeze after canceling the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· GE Healthcare, LLC

Recalled Item: Flow sensors that may be installed in the following GEHC Recalled by GE...

The Issue: The flow sensors built prior to June 2021 could have damaged tubes with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: uMI 550 System - Product Usage: intended to be operated Recalled by Shanghai...

The Issue: The EXAM acquisition workflow could occasionally freeze after canceling the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· GE Healthcare, LLC

Recalled Item: Flow sensors kept as stand-alone user replaceable spare parts for Recalled...

The Issue: The flow sensors built prior to June 2021 could have damaged tubes with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Gravity Burette Set 60 DROP 1.2 MF 2 SmartSite Recalled by CAREFUSION Due...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Gravity IV Set 3-port Closed Manifold Back Check Valve 3 Needle-Free...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD SE Burette Set 20 Drops 2 Injection Ports Vented/NonVented Recalled by...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Alaris Pump Infusion Buerette Set 0.2 Micron Filter Smallbore Recalled by...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES Recalled by...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD SmartSite Bag Access Device Recalled by CAREFUSION Due to Needle-free...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD SmartSite 'Y' Extension Set 2 Needle-Free Valves Recalled by CAREFUSION...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD BURETTE GRAVITY SET 60 DROP 2 Smartsite VALVES VENTED/NONVENTED Recalled...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD SmartSite Recalled by CAREFUSION Due to Needle-free connector valves,...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Syringe Set 20 DP MIC TBG 0.2MF CKV Anti-Siphon SmartSite VLV Sensing...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Gravity Burette Set 60 DP 3 SmartSite VALVES BALL VALVE DRIP CHAMBER...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD SmartSite Bag Access Device Needle-Free Valve Recalled by CAREFUSION Due...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing