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. 972 recalls have been distributed to North Dakota in the last 12 months.
Showing 25121–25140 of 47,938 recalls
Recalled Item: NxStage Express Fluid Warmer (FW-300 Recalled by NxStage Medical, Inc. Due...
The Issue: There is a potential risk of electrical fire when fluid leaks into the power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Seven Recalled by ESAOTE S.P.A. Due to The probe power monitoring...
The Issue: The probe power monitoring settings have been found to be not appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centron Product Usage: Vascular Recalled by Philips Healthcare Due to The...
The Issue: The first time an operator selects a new procedure type during a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper Product Usage: Vascular Recalled by Philips Healthcare Due to...
The Issue: The first time an operator selects a new procedure type during a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Gamma Recalled by ESAOTE S.P.A. Due to The probe power monitoring...
The Issue: The probe power monitoring settings have been found to be not appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Alpha Recalled by ESAOTE S.P.A. Due to The probe power monitoring...
The Issue: The probe power monitoring settings have been found to be not appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNIQ Product Usage: Vascular Recalled by Philips Healthcare Due to The first...
The Issue: The first time an operator selects a new procedure type during a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monsel's Solution (Ferric Subsulfate) Recalled by BioDiagnostic...
The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESTRADIOL 20mg PELLET Recalled by Qualgen, LLC Due to Labeling: Incorrect or...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irinotecan Hydrochloride Injection Recalled by Ingenus Pharmaceuticals Llc...
The Issue: Superpotent Drug: High out of specification assay value results for potency.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TESTOSTERONE 200 mg PELLET Recalled by Qualgen, LLC Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irinotecan Hydrochloride Injection Recalled by Ingenus Pharmaceuticals Llc...
The Issue: Superpotent Drug: High out of specification assay value results for potency.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MRSASelect Recalled by Bio-Rad Laboratories, Inc Due to Abnormal coloration...
The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRSASelect II Recalled by Bio-Rad Laboratories, Inc Due to Abnormal...
The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.