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. 925 recalls have been distributed to North Dakota in the last 12 months.
Showing 41121–41140 of 47,938 recalls
Recalled Item: Glytone Acne Recalled by Genesis Pharmaceutical, Inc. Due to Failed...
The Issue: Failed Stability Specifications: Out of specification results for viscosity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: triple therapy Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: This recall is due to out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PS-C Femoral Nonporous Rt Sz 6 Recalled by Ortho Development Corporation Due...
The Issue: A femoral component containing pegs was found in a box for the pegless version.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alligator Retrieval Device (ARD). Used in the peripheral and...
The Issue: Potential for the PTFE (polytetrafluoroethylene) coating to delaminate and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Medical Systems Computed Tomography X-ray systems (Brilliance CT...
The Issue: A customer reported that the table top had become free floating. A Field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRABECULAR METAL MODULAR ACETABULAR SYSTEM Recalled by Zimmer, Inc. Due to...
The Issue: The shell was missing the locking ring.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Linear Accelerator (LINAC) models. Product Usage: deliver X-ray...
The Issue: Siemens Radiation Oncology became aware that customers may be using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 550 TxT Treatment Table of the Digital Linear Accelerator (LINAC) Recalled...
The Issue: Table may lose calibration during patient treatment, which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pipeline Embolization Device (PED). Used endovascular treatment of adults...
The Issue: Potential for the PTFE (polytetrafluoroethylene) coating to delaminate and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Just Great Stuff Chocolate Dream Greens Recalled by Betty Lou's, Inc. Due to...
The Issue: Undeclared milk which was a contaminant of the dark chocolate ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EZ-IO 45mm (40kg & up) Needle Set Recalled by Vidacare Corporation Due to...
The Issue: The voluntary recall is due to the needle set not meeting its specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL¿ Anchor Peg Glenoid Plus (APG+) 2.5MM Breakaway Guide Pin Recalled by...
The Issue: Urgent Device Correction notifications are being sent to USA distributors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henora 300psi I.V. Catheter Extension Set Product Usage: Recalled by RGI...
The Issue: Problem with low adhesion of the tubing to luer connection which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Ant Recalled by Nova Products, Inc. Due to Undeclared Amounts
The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AFRICAN BLACK ANT Recalled by Nova Products, Inc. Due to Undeclared Amounts
The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MOJO RISEN Recalled by Nova Products, Inc. Due to Undeclared Amounts
The Issue: Marketed Without an Approved NDA/ANDA; Nova Products, Inc. of Aston,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xzone 1200 Recalled by Nova Products, Inc. Due to Undeclared Amounts
The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: XZEN PLATINUM Recalled by Nova Products, Inc. Due to Undeclared Amounts
The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: XZEN GOLD Recalled by Nova Products, Inc. Due to Undeclared Amounts
The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xzen 1200 Recalled by Nova Products, Inc. Due to Undeclared Amounts
The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.