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 21881–21900 of 27,512 recalls
Recalled Item: Philips Healthcare Brilliance 64 Computed Tomography X-ray system Recalled...
The Issue: During scans with specific protocol steps, the software unexpectedly sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity CT Computed Tomography X-ray system Recalled by...
The Issue: During scans with specific protocol steps, the software unexpectedly sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity Core Computed Tomography X-ray system Recalled...
The Issue: During scans with specific protocol steps, the software unexpectedly sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity Core 128 Computed Tomography X-ray system...
The Issue: During scans with specific protocol steps, the software unexpectedly sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...
The Issue: The internal blue flapper valve of certain KimVent Turbo-Cleaning Closed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remote Network Station Recalled by Nihon Kohden America Inc Due to Nihon...
The Issue: Nihon Kohden America (NKA) is recalling the Remote Network Station (RNS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Study and all acquired images deleted when using systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Medi-Pak Vaginal Speculum Recalled by CooperSurgical, Inc. Due to...
The Issue: Small sized specula were incorrectly packaged in printed bags for the medium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Ysio Max Recalled by Siemens Medical Solutions USA, Inc Due to Study...
The Issue: Study and all acquired images deleted when using systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Axiom Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Study and all acquired images deleted when using systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Uroskop Omnia Max Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Study and all acquired images deleted when using systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SynchroMed II Implantable Infusion Pumps Recalled by Medtronic...
The Issue: Medtronic is conducting a recall of a specific subset of Model 8637-20 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ 5 Ultrasound System with Pediatric Cardiology option Recalled by...
The Issue: When Epiq 5 Ultrasound System, WITH the Pediatric Cardiology option, is set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ 7 Ultrasound System with Pediatric Cardiology option Recalled by...
The Issue: When Epiq 7 Ultrasound System, WITH the Pediatric Cardiology option, is set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component Recalled by...
The Issue: Some rods may not meet the appropriate traceability requirements including...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TFN-ADVANCED Proximal Femoral Nailing System (TFNA) Recalled by Synthes,...
The Issue: TFNA nails from certain lots were assembled with a locking mechanism too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Primus (THE BTE WS30) Recalled by BTE Technologies, Inc. Due to On the...
The Issue: On the Primus that includes the optional Chop / Lift Bar, there is a remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MAX-CORE Disposable Core Biopsy Instrument Gauge x Length 18g Recalled...
The Issue: The firm is recalling Bard MAX-CORE Disposable Core Biopsy Instrument due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Malleable Penile Prosthesis Recalled by Coloplast Manufacturing US,...
The Issue: Several lots of the 9.5 mm Genesis Malleable Penile Prosthesis were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABACUS SE (Single-Workstation Edition) and ABACUS ME (Multi-Workstation...
The Issue: Baxter Corporation is conducting a field action for the ABACUS SE and ME...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.