Merit Medical recalls Blue Diamond Digital Inflation Devices with possible small holes in sterile barriers that could expose users to pathogens, leading to infection. Affected models include IN7152/C through IN7130/C with specific serial numbers and expiration dates.
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.
Merit Medical is recalling Blue Diamond Digital Inflation Devices that may have a small hole in the sterile barrier. This could expose users to pathogens and cause infection during use. Consumers should stop using affected devices immediately.
The devices may have a small hole in the sterile barrier, allowing pathogens or pyrogens to enter. Using these devices could lead to infections or other health complications during medical procedures.
Current users of Blue Diamond Digital Inflation Devices with the specific model numbers and serial numbers listed in the recall are affected. Medical professionals and patients using these devices for procedures are at highest risk.
Check the product's model number (IN7152/C, IN7352/C, IN7403/C, IN7802/C, IN7852/C, or IN7130/C) and the specific serial numbers or expiration dates listed in the recall notice.
Immediately stop using any Blue Diamond Digital Inflation Device with the model numbers and serial numbers listed in the recall.
Models IN7152/C, IN7352/C, IN7403/C, IN7802/C, IN7852/C, and IN7130/C with specific serial numbers and expiration dates listed in the recall.
Check the product's model number and serial numbers against the list provided in the recall notice, which includes specific expiration dates and lot numbers.
Stop using the device immediately and contact Merit Medical for further instructions.
We’ve drafted a message you can send Merit Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0064-2025 — Merit Medical Merit Medical Hello, I own a Merit Medical that is covered by recall Z-0064-2025 from Merit Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
