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All product recalls associated with MasterPharm LLC.
Total Recalls
1000
Past Year
353
Class I (Serious)
22
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Lack of Processing Controls (lack of assurance of conformity to specifications).
A recent FDA inspection at the firm identified that the foil test performed during installation of the device does not have clear acceptance criteria.
The perforated screen that divides the inside of the process water tank has a very sharp edge across the top of the Heat Exchanger leading to potential injury for servicer.
Software defect may result in disapperance of tag sites during recalculation and lead to additional ablation sites. This may lead to prolongation of the procedure and, in extremely rare circumstances, cardiac perforation.
The locking mechanism at the interface of the Instrument Carrier and the Leksell Vantage Arc may not function properly.
Super-potent Drug: This recall has been initiated due to the elevated presence of minoxidil and biotin.
When using Sample Transfer protocol version 3.0, the drop catcher is not activated on the MagNA Pure 96 instrument, which introduces a potential risk for cross-contamination leading to erroneous results.
Lateromedial (LM) and Lateromedial Oblique (LMO) Orientation Markers may be displayed incorrectly on the 3D TOMO slider bar. In addition, the slice location of the image and/or the slice direction could be incorrect as well, and result in misdiagnosis
Possible unintended interruption of surgical procedures due to equipment shutdown, related to changes in voltage.
Daimler Trucks North America LLC (DTNA) is recalling certain 2019-2021 Western Star 4700 and 5700 vehicles. A particular wire in the ground harness may be undersized, possibly resulting in a melted connector in the ground circuit harness. If the connector becomes damaged, under certain circumstances, the engine may stall without the ability to restart.
Couch Correction moves sent after using a 3D CT scan are partially lost if the previous correction sent or recorded had some of the Couch Correction checkboxes turned off
McNeilus Truck & Manufacturing, Inc. (McNeilus) is recalling certain CNG Fuel Systems that it sold as aftermarket parts. These systems, part number 2702100, include an EMER thermally activated pressure relief device. The pressure relief devices (PRDs) may not vent the system when exposed to heat, potentially resulting in the system rupturing.
Mapping Catheter can become entrapped in the cardiac valvular apparatus while the user is attempting to create an electroanatomic map.
Mapping Catheter can become entrapped in the cardiac valvular apparatus while the user is attempting to create an electroanatomic map.
Spartan Motors, Inc. (Spartan) is recalling certain 2020-2021 FLT Utilimaster Truck Body vehicles. The license plate lamp may be installed in the incorrect position and at an incorrect angle, causing the plate to not be properly illuminated. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices, and Associated Equipment."
The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris.
Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules were found to contain minoxidil.
Restorations crack during the sintering process.
The surgical gowns were manufactured in a facility that is not registered by the FDA.
The surgical gowns were manufactured in a facility that is not registered by the FDA.