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. 2,375 recalls have been distributed to North Dakota in the last 12 months.
Showing 23161–23180 of 27,512 recalls
Recalled Item: Philips IP5 Information Portal The Expression Information Portal (Model IP5)...
The Issue: The wireless function of the IP5 radio could be interrupted causing loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance 1227 Cart and Utensil Washer/Disinfector Product Usage: Usage: The...
The Issue: STERIS has identified that deformation of the washers door handle pin may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life Force Chamber Product Usage:The product is intended for restful...
The Issue: The Life Force chamber is marketed and promoted as a medical device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Data Manager 2.0 (Content manager 2.0 Recalled by Brainlab AG Due to...
The Issue: The following defects have been identified for data loaded with Patient Data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The STERIS 4085 General Surgical Table Product Usage: is an Recalled by...
The Issue: STERIS engineering analysis has determined the D1 pressure switch in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solanas 2.1mm FIXED DEPTH DRILL Recalled by Alphatec Spine, Inc. Due to...
The Issue: Alphatec Spine is recalling the 2.1mm Fixed Depth Drill 10mm because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affinity¿ Four Birthing Bed Recalled by Hill-Rom, Inc. Due to The attachment...
The Issue: The attachment latch mechanism can become bent depending on user handling....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esaote PA230E Transducer A portable and cart base ultrasound system Recalled...
The Issue: Using the PA230E transducer with a user-defined setting with the output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The synthetic non-absorbable surgical sutures CARDIOFLON Evolution are...
The Issue: A potential splitting of the surface treatment of the thread ends on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The synthetic non-absorbable surgical sutures CARDIOXYL are composed of a...
The Issue: A potential splitting of the surface treatment of the thread ends on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Essential NEO Recalled by Karl Storz Endoscopy Due to KARL STORZ...
The Issue: KARL STORZ Endoscopy-America is recalling the Essential NEO because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology Hemo. McKesson Cardiology" Hemo is intended for complete...
The Issue: McKesson Cardiology Hemo front-end parameter boxes must undergo annual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxygen Mask Recalled by Salter Labs Due to The case label correctly states...
The Issue: The case label correctly states partial rebreather but the insert label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Tapered Screw-Vent Implant Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Dental is conducting a voluntary recall of a single lot of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MK5 NX Controller--Wheelchair controller Recalled by Invacare Corporation...
The Issue: M41 Powered Wheelchairs received through Invacare Service Parts (ISP) have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonopet Ultrasonic Surgical System Console Recalled by Stryker Instruments...
The Issue: The firm received complaints regarding insufficient irrigation to the tip of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Peripherally Inserted Central Catheter (PICC) and Dialysis catheter...
The Issue: Potential for inadvertent scalpel stick injury involving the safety scalpel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT: product code 882482 Recalled by Philips Medical Systems...
The Issue: Flat Panel Display (FPD) failed to remain securely locked in the deployed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis EMPIRA RX PTCA Dilatation Catheter Recalled by Cordis Corporation Due...
The Issue: The balloon may exhibit resistance to the removal of the balloon cover....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis EMPIRA NC RX PTCA Dilatation Catheter Recalled by Cordis Corporation...
The Issue: The balloon may exhibit resistance to the removal of the balloon cover....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.