Merit Medical Systems, Inc. recalls basixTOUCH Inflation Device, REF: IN8140/A
Recalled Product
basixTOUCH Inflation Device, REF: IN8140/A
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): IN8140/A/00884450627105/H2925218(4/22/2027), H2929411(4/29/2027), H2938003(4/30/2027), H2972592(4/30/2027), H2982505(12/31/2026).
View official government recall
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