Recalled International Medsurg Piston Syringes and Hypodermic Needles due to insufficient documentation supporting product sterility claims. Affected units include specific lot numbers and quantities.
Insufficient documentation to support product sterility claims.
International Medsurg is recalling piston syringes and hypodermic needles that lack proper sterility documentation. This could lead to infections if used for medical procedures.
The products do not have sufficient documentation to confirm they are sterile. Using non-sterile medical devices can introduce harmful bacteria into the body, potentially causing infections.
Healthcare professionals and individuals using these medical devices for injections or fluid withdrawal. Those with the specific lot numbers listed are most at risk.
Check for the product name 'Piston Syringe and Hypodermic Needle, 3 CC L/L 25 G X 1.0, 100 per box' with the listed lot numbers (e.g., 12-6780-x, 12-6925-x, etc.).
Look for the specific lot numbers listed in the recall notice to determine if your product is affected.
The products lack sufficient documentation to support sterility claims, which could lead to infections if used for medical procedures.
Check the product lot numbers against the list provided in the recall notice to see if it is affected. If it is, you should stop using it and contact the manufacturer.
Using non-sterile medical devices can introduce harmful bacteria into the body, potentially causing infections. However, the recall does not specify a risk of serious injury.
We’ve drafted a message you can send International Medsurg to request your refund or repair — edit it as you like.
Subject: Recall Z-2836-201 — International Medsurg International Medsurg Hello, I own a International Medsurg that is covered by recall Z-2836-201 from International Medsurg. 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.
