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. 2,363 recalls have been distributed to North Dakota in the last 12 months.
Showing 26301–26320 of 27,512 recalls
Recalled Item: Giraffe and Panda Bag and Mask Resuscitation System The T-piece Recalled by...
The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare - Giraffe and Panda T-Piece Resuscitation System The Recalled...
The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The SYMBIONIC LEG is an integrated prosthetic leg for transfemoral Recalled...
The Issue: OSSUR is recalling the Symbionic Leg because it is not recognizing the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Enteralite Ambulatory Feeding Pumps Recalled by MOOG Medical...
The Issue: The firm is adding an addendum to the operator's manual for Infinity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Discovery NM/CT670 Recalled by GE Healthcare, LLC Due to GE Healthcare...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Liberty Cycler Set Single Conn. Ext. DL. Part Number: Recalled by...
The Issue: There is a small risk of a leak in Cycler Sets and if the Cycler Set is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens StreamLAB(R) Analytical Workcell Recalled by Siemens Healthcare...
The Issue: Firm has received reports from customers that the small pins at the bottom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Stryker Model 6390 Recalled by Stryker Medical Division of Stryker...
The Issue: Model 6390 Power-LOAD systems built between September 12, 2012 and September...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista(R) Alkaline Phosphatase (ALP) Calibrator The ALP CAL...
The Issue: Correlation slope bias and accuracy shift
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Mobilette Mira Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: There is a risk of lost images during examination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAVIG PORTEGRA 2 system operated in conjuction with a Siemens Recalled by...
The Issue: A particular component may not have been fitted during the installation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alfa Wassermann System Diluent 750 mL Manufactured for Alfa Wassermann...
The Issue: Inorganic phosphorus assays using System Diluent Lot 155599 may not product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTRA C200 Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...
The Issue: Horiba Medical is recalling the ABX PENTRA AST CP because during the AST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA AST CP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...
The Issue: Horiba Medical is recalling the ABX PENTRA AST CP because during the AST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Ferritin Calibrator C-Used with the ADVIA Centaur Ferritin...
The Issue: Ferritin Analytical Sensitivity and Calibrator C Realignment with kit lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Calibrator C-Used with the ADVIA Centaur Ferritin assay...
The Issue: Ferritin Analytical Sensitivity and Calibrator C Realignment with kit lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Calibrator C-Used with the ADVIA Centaur Ferritin assay...
The Issue: Ferritin Analytical Sensitivity and Calibrator C Realignment with kit lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate Membrane units for E7077 Electrode Radiometer Medical ApS. The...
The Issue: RADIOMETER became aware that some membranes may have enzyme residue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The touchscreen display (model 94267) designed for use with the Recalled by...
The Issue: Potential failure of Spacelabs Healthcare Touchscreen Display, Model 94267...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle3 VCC P/N 4598 001 41341 REV A Recalled by Philips Medical Systems...
The Issue: Philips Medical Systems Cleveland), Inc. is recalling Pinnacle3 Virtual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.