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. 1,662 recalls have been distributed to North Dakota in the last 12 months.
Showing 46661–46680 of 47,938 recalls
Recalled Item: Breath Tech Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFlow Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Resuscitator Recalled by Ventlab Corporation Due to Possible volume...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Rescue Med Infant Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Premium Small Adult Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V*Care Resuscitator Infant Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFlow Resuscitator Recalled by Ventlab Corporation Due to Possible volume...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MultiDiagnost Eleva with Flat Detector (MD Eleva FD)Model: 708034...
The Issue: When doing a 3 Dimensional Rotational Angiography (3DRA) the 3D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Premium Small Child Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stat-Check Resuscitator Recalled by Ventlab Corporation Due to Possible...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Narrow CrossFit (NC) Screw for CARES Abutment ZrO2. Endosseous...
The Issue: Incorrect Screw (RC) included with NC CARES Abutment Set was not a Narrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe Spot Infant Resuscitator Recalled by Ventlab Corporation Due to...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Transdermal System Recalled by Actavis Due to Subpotent; some...
The Issue: Subpotent; some patches may not contain fentanyl gel
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMPAX CV Reporting The Results Management (RM)/IMPAX CV reporting component...
The Issue: When users selected "Left stenosis" in the "Graft Duplex Conclusion" section...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chromovision High Definition (HD) Wireless Camera Recalled by Berchtold...
The Issue: Defective camera: There is a possibility that the connection of the wires to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima XR200amx. Mobile general purpose radiographic imaging of the human...
The Issue: Software issue: a violation of 21 CFR 1020.31(a). After an image is taken,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima XR220amx Mobile general purpose radiographic imaging of the human...
The Issue: Software issue: a violation of 21 CFR 1020.31(a). After an image is taken,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beekley A-Spots Floral Skin Markers -Order Number: 751 Product Usage:...
The Issue: Digital Skin Mammography Marker separating from the backing of the spot material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beekley O-Spots Floral Skin Markers -Order Number: 752 Product Usage:...
The Issue: Digital Skin Mammography Marker separating from the backing of the spot material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IRISpec" CA/CB two-part urine chemistry control twin set Recalled by Iris...
The Issue: The firm recalled after it received complaints of IRISpec CA/CB two part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.