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. 2,540 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,540 in last 12 months

Showing 67816800 of 27,512 recalls

Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Ultra-Fine Insulin Syringe 0.5mL Recalled by Becton Dickinson & Company...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Synthes (USA) Products LLC

Recalled Item: TFN-Advanced Femoral Nail 12MM/125 DEG TI CANN TFNA 200MM STERILE. Recalled...

The Issue: TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: Power-PRO 2 . Intended as an ambulance cot to transport Recalled by Stryker...

The Issue: Transport Cot has insufficient volume of epoxy to assemblies installed in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Ultra-Fine II Insulin Syringe 0.5mL Recalled by Becton Dickinson &...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Synthes (USA) Products LLC

Recalled Item: TFN-Advanced Femoral Nail 12MM/125 DEG TI CANN TFNA 170MM - Recalled by...

The Issue: TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Scientia Vascular, Inc.

Recalled Item: Plato 17 Microcatheter: Straight Tip Recalled by Scientia Vascular, Inc. Due...

The Issue: Microcatheters for embolic coil and diagnostic agent introduction to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Insulin Syringes with the BD Micro-Fine IV Needle 1 ml Recalled by Becton...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Ultra-Fine Insulin Syringe 1mL Recalled by Becton Dickinson & Company Due...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Ultra-Fine Insulin Syringe 1mL Recalled by Becton Dickinson & Company Due...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· BioFire Diagnostics, LLC

Recalled Item: In Vitro Diagnostic (IVD) Panel BioFire BCID2 Panel - Recalled by BioFire...

The Issue: Due to temperature excursions with products (products being stored outside...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· BioFire Diagnostics, LLC

Recalled Item: In Vitro Diagnostic (IVD) Panel BioFire Respiratory Panel 2.1 (RP2.1)...

The Issue: Due to temperature excursions with products (products being stored outside...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Insulin Syringes with the BD Micro-Fine TM IV Needle 1ml Recalled by...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· BioFire Diagnostics, LLC

Recalled Item: In Vitro Diagnostic (IVD) Panel FilmArray GI Panel - Recalled by BioFire...

The Issue: Due to temperature excursions with products (products being stored outside...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Synthes (USA) Products LLC

Recalled Item: TFN-Advanced Femoral Nail 12MM/130 DEG TI CANN TFNA 170MM STERILE. Recalled...

The Issue: TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Preat Corp

Recalled Item: PREAT NOBIL GRIP Recalled by Preat Corp Due to Product is labeled with an...

The Issue: Product is labeled with an incorrect expiration date.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceFebruary 1, 2023· Aniara Diagnostica LLC

Recalled Item: BIOPHEN Protein C 5 kit is for in vitro quantitative Recalled by Aniara...

The Issue: New warnings and precautionary statements on product labelling: Reagent 2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution Recalled by...

The Issue: MiniCap Disconnect Cap with Povidone-Iodine are packaged in foil pouches,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· Maquet Cardiovascular, LLC

Recalled Item: Fusion Bioline Vascular Graft Recalled by Maquet Cardiovascular, LLC Due to...

The Issue: One (1) Fusion Bioline Vascular graft from lot 25162546, which failed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Tacrolimus (TAC) Flex reagent cartridge-In vitro diagnostic test...

The Issue: Siemens Healthineers has received customer complaints and confirmed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· DiaSorin Molecular LLC

Recalled Item: Simplexa COVID-19 Direct Recalled by DiaSorin Molecular LLC Due to Direct...

The Issue: Direct amplification Discs , used with COVID-19 and Flu A/B & RSV assays,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing