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. 2,404 recalls have been distributed to North Dakota in the last 12 months.
Showing 19961–19980 of 27,512 recalls
Recalled Item: Short Percutaneous Antenna with Thermosphere" Technology Standard...
The Issue: Medtronic is voluntarily recalling specific item codes and production lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G4 PLATINUM Receiver with Share Receiver Part Number: MT22495...
The Issue: Customers may not receive an intended audible alarm or alert if relying on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G4 PLATINUM (Pediatric) Receiver Receiver Part Number: MT22430...
The Issue: Customers may not receive an intended audible alarm or alert if relying on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium Low Profile Neuro Screw Recalled by Synthes (USA) Products LLC Due...
The Issue: Out of specification at the thread. The thread height of these screws is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Video Duodenoscope Recalled by Pentax Medical Company Due to Pentax Medical...
The Issue: Pentax Medical learned of reports of carbapenem-resistant Enterobacteriaceae...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molteno3 Glaucoma Implants G-Series: GS-Single Plate 175mm2 (IOP reorder#:...
The Issue: Innovative Ophthalmic Products (IOP) is recalling the Molteno 3 G-Series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX Pentra 400 (version 5.0.8 or lower) The ABX PENTRA Recalled by Horiba...
The Issue: Horiba Instruments, Inc. is recalling ABX Pentra 400( version 5.0.8 or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis (system Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Possible leak in the cooling system, fluids could potentially seep into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/zeego (system Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Possible leak in the cooling system, fluids could potentially seep into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software issues on Cios Alpha mobile C-Arm system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentra C400 (version 1.1.2 or lower) The ABX PENTRA 400 Recalled by Horiba...
The Issue: Horiba Instruments, Inc. is recalling ABX Pentra 400( version 5.0.8 or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sure Vue Color Staph 150T Recalled by Integrated Science Systems Inc Due to...
The Issue: Customer complaints of very weak reactions with the kit, or false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis zee/zeego Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis zee/zeego Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oblique Posterior Atraumatic Lumbar (OPAL) System Recalled by Synthes (USA)...
The Issue: The label on the outer packaging does not match the product inside and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) VITROS¿ Immunodiagnostic Products Total Beta-hCG II Reagent Pack (Unique...
The Issue: When testing was conducted using certain lots, VITROS¿ Systems generated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Horizon Medical Imaging (HMI) products versions 4.6.1 to including...
The Issue: McKesson has identified a design deficiency where under rare circumstances,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...
The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...
The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...
The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.