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All product recalls associated with UTILIMASTER.
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.
Shyft Group is recalling certain 2023 Utilimaster Upfit vehicles. The battery cable connections for the electrical harness may be connected incorrectly, causing the circuit protection on the cables to be ineffective.
Artificial hearts contain a epoxy resin that has not been reviewed by the FDA for safety and efficacy.
A crack in the weld of the rasp handle may lead to a fracture of the frontal sleeve when the rasp is further impacted or extracted. The rasp remains intact. The rasp would need to be pulled out by a clamp leading to a prolongation of surgery or modified surgery
Trocar manufactured with the shaft too long and does not meet manufacturing specifications. As a result, when used with the 30 neuroendoscope, a portion of the visual field is obscured.
Philips has become aware of the potential for unintended radiation exposure with Zenition 70 systems with Vascular Extension option and a Wireless Foot Switch.
A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation
A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation
A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation
Product is labeled with incorrect offset.
May have a battery life lasting less than the full 48 hours, requiring the device to be charged more frequently.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Increased force may be required to remove the LINK MP Monoblock trial hip stem (Sizes 14mm - 25mm),after impaction. Potential for prolongation of surgery or the surgical procedure may have to be modified due to this issue
Loss of availability of the wireless foot switch during procedures.
Potential failure of a bearing adhesive joint that can occur due to an assembly issue of the X/Y stage of the handpiece. If a broken glue bond were to occur, it could cause an overlap of cores, potentially leading to prolonged healing and irregularities in patient skin texture post-treatment, and/or scarring
This recall involves Poseidon M28A Dive Computers used for diving. They calculate continuously and present needed data for divers. The M28A works stand alone or in combination with the Poseidon SE7EN Rebreather. Only dive computers with a serial number starting with "M28A-" are included in this recall. The serial number and two metallic wet-switches are located on the back side of the recalled dive computers.
The C-arm, used to set the position and angle of the x-ray exposure field, may not function due to the tableside console PWB, which needs replacement. There may be a delay in the procedure, but procedures can continue using the operators console, the switches on the back of the column, switches on the side of the flat panel detector, and the emergency stop will continue to function normally.