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. 2,026 recalls have been distributed to North Dakota in the last 12 months.
Showing 2321–2340 of 47,938 recalls
Recalled Item: Instant Milk Tea Matcha Flavor Recalled by R&M TRADING LLC Due to The...
The Issue: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Instant Milk Tea Taro Flavor Recalled by R&M TRADING LLC Due to The Instant...
The Issue: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy...
Recommended Action: Do not consume. Return to store for a refund or discard.
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.
Recalled Item: Instant Milk Tea Honeydew Flavor Recalled by R&M TRADING LLC Due to The...
The Issue: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy...
Recommended Action: Do not consume. Return to store for a refund or discard.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: GCE HEALTHCARE Zen-O lite Recalled by Ohio Medical Corporation Due to...
The Issue: Erroneous calibration values, potentially resulting in: as the device ages,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name [REF]: Supply Server Recalled by CareFusion 303, Inc. Due to...
The Issue: During automated dispensing cabinet upgrade/installation/reimaging,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.