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. 2,573 recalls have been distributed to North Dakota in the last 12 months.
Showing 1001–1020 of 27,512 recalls
Recalled Item: Medical convenience kits IHDC30R D AND C PACK Recalled by American Contract...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits UDPG88W PICC G-TUBE PACK-230209 Recalled by...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XERF EFFECTOR 60. Electrosurgical unit. Recalled by Lutronic Corporation Due...
The Issue: Manufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description ANCV78BC HEART PACK -...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description LKRA40G RADIOLOGY PACK...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item number/ Product description AKGN82E GENERAL...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description BFCT04X CATARACT PACK -...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description BUCY78E CYSTO PACK CMCP10X...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item number/ Product description AHLD15X LABOR...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description RCEN25B ENT SDSC 0246972...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description RCGY52D GYN LAPAROSCOPY SPH...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description UICL44P ADULT CENTRAL LINE...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: The BIOS battery may deplete faster than initially anticipated during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/15 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: The BIOS battery may deplete faster than initially anticipated during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: The BIOS battery may deplete faster than initially anticipated during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: The BIOS battery may deplete faster than initially anticipated during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Potential issue that can cause the device to register "phantom" touches in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: The BIOS battery may deplete faster than initially anticipated during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: The BIOS battery may deplete faster than initially anticipated during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10C Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: The BIOS battery may deplete faster than initially anticipated during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.