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. 949 recalls have been distributed to North Dakota in the last 12 months.
Showing 36421–36440 of 47,938 recalls
Recalled Item: Apex ARC Hip Stem Recalled by Omnilife Science Inc. Due to Product may...
The Issue: Product may breach the inner and outer sterile pouches during shipping or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Medley LVP Bezel Assembly. Intended use to hold platen Recalled by...
The Issue: Administration of inappropriate quantities of fluid can result, with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Femoral Drill Guide Lateral IM Adapter Product Usage: Drill Recalled...
The Issue: Oxford Femoral Drill Guide Lateral IM Adapter may have an undersized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING FEMORAL HEAD Recalled by...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Medley LVP Frame Membrane. Intended use to hold platen Recalled by...
The Issue: Administration of inappropriate quantities of fluid can result, with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING ACETABULAR CUP W/IMPACTOR...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING DYSPLASIA CUP W/IMPACTOR...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WIZARD2 2-detector Recalled by Perkinelmer Due to Error in WIZARD2 Barcode...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...
The Issue: Multiple dietary supplement regulation violations.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Stryker SelectCore Variable Throw Biopsy Device Recalled by Stryker...
The Issue: Stryker Instruments is recalling the Stryker SelectCore Variable Throw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurus 2500 Standalone Vitreous Probe Recalled by Alcon Research, Ltd. Due...
The Issue: Insufficient seal on the outside packaging, potentially affecting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVac 70 XTRA with Integrated Cable and PROcise EZ View Recalled by...
The Issue: Wands inspected with the adaptor fixture were released to the field not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Testosterone 25 mg Recalled by The Compounding Pharmacy of America Due to...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl 2 Recalled by The Compounding Pharmacy of America Due to Lack of...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl 8 Recalled by The Compounding Pharmacy of America Due to Lack of...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glutathione 200 mg/ml Injection Recalled by The Compounding Pharmacy of...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.