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. 2,531 recalls have been distributed to North Dakota in the last 12 months.
Showing 9921–9940 of 27,512 recalls
Recalled Item: BIOTRONIK Ilestro 7 VR-T Recalled by BIOTRONIK Inc Due to There is a...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK Ilestro 7 DR-T Recalled by BIOTRONIK Inc Due to There is a...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK Iforia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK INTICA NEO 7 HF-T DF-1 IS-1 ProMRI Recalled by BIOTRONIK Inc Due...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK Iforia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK Iperia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK ILIVIA NEO 7 VR-T DF-1 ProMRI Recalled by BIOTRONIK Inc Due to...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK INVENTRA 7 Recalled by BIOTRONIK Inc Due to There is a potential...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK INTICA NEO 7 VR-T DX DF-1 ProMRI Recalled by BIOTRONIK Inc Due to...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK INVENTRA 7 Recalled by BIOTRONIK Inc Due to There is a potential...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK IPERIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow OnControl Bone Lesion Biopsy System Tray-11 ga 10 cm Recalled by Arrow...
The Issue: Difficulty inserting the biopsy ejector rod into the bone lesion biopsy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i (RoHS) Dual Aspirate Autosampler (SMN 11219530) - OUS Recalled...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAMBA Flex 135 Microcatheter. Packaged with protective sleeve over catheter...
The Issue: The firm initiated a removal of certain batches of MAMBA 135 and MAMBA Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i (RoHS) with Single Aspirate Autosampler (SMN 11219529) - US...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.