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. 2,380 recalls have been distributed to North Dakota in the last 12 months.
Showing 22141–22160 of 27,512 recalls
Recalled Item: G7 Variant Elution Buffer HiS no. 1 (M) component of Recalled by Tosoh...
The Issue: The G7 Variant Elution Buffer HiS no. 1 (M) is incorrectly labeled with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical PESSARY KIT-CUBE#2 Recalled by CooperSurgical, Inc. Due to...
The Issue: Incorrect size printed on the Milex Pessary Kit packaging label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DigitalDiagnost System X-Ray Recalled by Philips Medical...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DuraDiagnost X- Ray Recalled by Philips Medical Systems,...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo HX2 Temperature Management System provides temperature control of two...
The Issue: Malfunctioning mixing valve and loss of cooling and/or heating capability....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS SOMATOM Force with software version VA50A and /or VA50A_FP1 Recalled...
The Issue: Possibility of image artifacts during data acquisition when using Adaptive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems Ingenuity Core. Intended to produce...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems Brilliance CT 64-channel with Essence...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems Ingenuity CT scanners. Intended to produce...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zip 8M Wound Closure Device Recalled by Zipline Medical Due to The...
The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DermaPen Pro Model Recalled by Derma Pen, LLC Due to Derma Pen initiated a...
The Issue: Derma Pen initiated a field communication for Dermapen after receiving an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray systems Brilliance iCT Recalled by Philips Medical...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems (Brilliance CT 64-channel w/Essence...
The Issue: Philips discovered that a software defect exists in marketed product wherein...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Legionella BCYE Growth Supplement SR0110A packaged in packs of...
The Issue: Use of the product may not provide adequate recovery and could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zip 8i Surgical Skin Closure Device Recalled by Zipline Medical Due to The...
The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems Ingenuity Core 128. Intended to produce...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zip 16 Surgical Skin Closure Device Recalled by Zipline Medical Due to The...
The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems Brilliance iCT SP. Intended to produce...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW FiberOptix Intra-Aortic Balloon Catheter Kit Recalled by Arrow...
The Issue: Outer package product label incorrectly identifies the product as FiberOptix...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Synapse Cardiovascular I ProSolv CardioVascular Synapse...
The Issue: Under certain circumstances the patient Demographics in a report exported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.