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. 2,573 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,573 in last 12 months

Showing 23212340 of 47,938 recalls

Medical DeviceMay 12, 2025· BD SWITZERLAND SARL

Recalled Item: BD Texium Needle-Free Syringe: 3 mL Recalled by BD SWITZERLAND SARL Due to...

The Issue: Sterile, single use closed system drug transfer devices, standalone or on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Novum IQ Syringe Pump Recalled by Baxter Healthcare Corporation Due...

The Issue: Baxter has identified a design issue which may cause the pump to detect the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2025· BD SWITZERLAND SARL

Recalled Item: BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP Recalled by BD SWITZERLAND SARL...

The Issue: Sterile, single use closed system drug transfer devices, standalone or on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2025· BD SWITZERLAND SARL

Recalled Item: Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium...

The Issue: Sterile, single use closed system drug transfer devices, standalone or on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2025· BD SWITZERLAND SARL

Recalled Item: BD Texium: 3 mL Recalled by BD SWITZERLAND SARL Due to Sterile, single use...

The Issue: Sterile, single use closed system drug transfer devices, standalone or on...

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

Class II — Potential Health HazardOngoing
FoodMay 9, 2025· Homegrown Family Foods LLC

Recalled Item: Shore Lunch BREADING & BATTER MIX OVEN STYLE A savory Recalled by Homegrown...

The Issue: Undeclared Milk.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugMay 9, 2025· AvKARE

Recalled Item: Chlorthalidone Tablets Recalled by AvKARE Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 9, 2025· Alembic Pharmaceuticals Limited

Recalled Item: Celecoxib Capsules Recalled by Alembic Pharmaceuticals Limited Due to...

The Issue: Presence of Foreign Tablets/Capsules; customer complaint found one Tadalafil...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 9, 2025· KVK Tech, Inc.

Recalled Item: Indomethacin Extended-Release Capsules USP Recalled by KVK Tech, Inc. Due to...

The Issue: cGMP deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 9, 2025· KVK Tech, Inc.

Recalled Item: Phentermine Hydrochloride Capsules Recalled by KVK Tech, Inc. Due to cGMP...

The Issue: cGMP deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 9, 2025· Philips Respironics, Inc.

Recalled Item: BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for...

The Issue: This device does not indicate for use in patients with respiratory failure.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 9, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Brand Name: VITROS Recalled by Ortho-Clinical Diagnostics, Inc. Due to a...

The Issue: a software anomaly allows test results to be reported using Micro Tip and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2025· Philips Respironics, Inc.

Recalled Item: BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory...

The Issue: This device does not indicate for use in patients with respiratory failure.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 9, 2025· Philips Respironics, Inc.

Recalled Item: BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support...

The Issue: This device does not indicate for use in patients with respiratory failure.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 9, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Brand Name: VITROS Product Name: VITROS 4600 Chemistry System Model/Catalog...

The Issue: a software anomaly allows test results to be reported using Micro Tip and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Brand Name: VITROS Product Name: VITROS 5600 Integrated System Model/Catalog...

The Issue: A software anomaly allows test results to be reported using Micro Tip and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2025· Barco N.V.

Recalled Item: Model: Description/: MNA-420 ENC -H/K9303320 Recalled by Barco N.V. Due to...

The Issue: Cathode ray tube display system encoders and decoders have same MAC address;...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2025· Baxter Healthcare Corporation

Recalled Item: 2.5 V replacement rechargeable batteries for Hillrom WELCH ALLYN PocketScope...

The Issue: The replacement rechargeable batteries inserted into the Welch Allyn...

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

Class II — Potential Health HazardOngoing
FoodMay 8, 2025· Now Foods

Recalled Item: NOW Nutritional Yeast Powder Recalled by Now Foods Due to regular yeast was...

The Issue: regular yeast was inadvertently packaged as nutritional yeast

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceMay 8, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis Product Name / UDI-DI code / Catalog No. Recalled by CareFusion...

The Issue: Antivirus software was not consistently installed on impacted devices during...

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

Class II — Potential Health HazardOngoing