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. 1,989 recalls have been distributed to North Dakota in the last 12 months.
Showing 6521–6540 of 47,938 recalls
Recalled Item: VA-LCP Clavicle Plate 2.7 Recalled by Synthes (USA) Products LLC Due to...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5MM Drill Bit/QC/85MM Sterile-surgical Recalled by Synthes (USA) Products...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TFNA Femoral Nail 9mm Recalled by Synthes (USA) Products LLC Due to Products...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13 mm Titanium Hindfoot Arthrodesis Cannulated Nails EX Recalled by Synthes...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Opal Recalled by Synthes (USA) Products LLC Due to Products not sterilized,...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Erythropoietin (EPO) Assay (100 Test) Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed an average negative bias of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Erythropoietin (EPO) Assay (100 Test) Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed an average negative bias of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: impression coping Recalled by Thommen Medical AG Due to The depth of the...
The Issue: The depth of the internal canal was not manufactured according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Safe Lock Catheter Ext. 12 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVS Health Waterproof Wound Tracking Dressing Recalled by MEDLINE...
The Issue: Product failed sterility testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Luer Lock Adapter 4 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Luer Lock Catheter Ext. 18 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Luer Catheter Ext. 6 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Luer Lock Catheter Ext. 12 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norepinephrine Bitartrate in 5% Dextrose Injection Recalled by Baxter...
The Issue: Incorrect product concentration on the overwrap label: The overwrap label...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS XT7600 Integrated System Recalled by Ortho-Clinical Diagnostics, Inc....
The Issue: Potential For Aspiration from Unintended Sample Container During Sampling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Battery Mobile X-ray Unit EASY MOVING Model with telescopic column 3.1...
The Issue: Potential interference with the anti-fall system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy Recalled by B. Braun...
The Issue: Kits should contain Filter Straws with Standard Luer Connections however the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy Recalled by B. Braun...
The Issue: Kits should contain Filter Straws with Standard Luer Connections however,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Duet External Drainage and Monitoring System Recalled by Medtronic...
The Issue: Potential for catheter disconnection from the patient line stopcock connectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.