Product Recalls in Montana
Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,306 recalls have been distributed to Montana in the last 12 months.
Showing 41521–41540 of 48,326 recalls
Recalled Item: Circular Lock Screws Recalled by Genesys Orthopedics Systems, LLC Due to The...
The Issue: The recall is being initiated because MK Precision (the Circular Lock Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABACUS TPN Calculation Software Recalled by Baxter Corporation Englewood Due...
The Issue: 1. ABACUS v3.1 may calculate quantities of electrolytes that are double the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ACUSON X700 Ultrasound Systems with software version 1.0.00 Recalled...
The Issue: When fourSight 4D ultrasound imaging, 3-Scrape real time 3D imaging, or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Potential safety issue...
The Issue: Potential safety issue with gradient coil electromechanical connections...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor with system software version...
The Issue: Software communication failure may occur on the HeartStart XL+ locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydrOXYzine Hydrochloride Oral Solution Recalled by Hi-Tech Pharmacal Co.,...
The Issue: Failed Impurity/Degradation Specification; out-of-specification result for...
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: Metoprolol Succinate Extended-Release Tablets Recalled by Wockhardt Usa Inc....
The Issue: Failed Dissolution Specifications: failure of dissolution test observed at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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.