FDAAugust 19, 2024device

MONARCH Inflation Device, REF: IN2430/B, IN2530/B, IN2130/B

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

merit medical systemsmeritmerit medical

UPCs

008844502980530088445029806000884450298022

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →