Merit Medical Systems, Inc. recalls BlueFIRE Inflation Device, REF: IN10140
Recalled Product
BlueFIRE Inflation Device, REF: IN10140
Hazard / Issue
Inflation devices may have a small hole in the sterile barrier of the device and use of affected devices may result in exposure to pathogens/pyrogens which could lead to infection.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: REF/UDI-DI/Lot(Expiration): IN10140/00884450363607/H2934827(4/30/2027)
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