medical Class II Updated 2024-10-23

Merit Medical Systems, Inc. recalls IntelliSystem Inflation Device, REF: IN1525/D

Recalled Product

IntelliSystem Inflation Device, REF: IN1525/D


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): IN1525/D/00884450298015/ H2918426(4/22/2027), H2934697(1/31/2027)
View official government recall

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