International Medsurg recalls 60cc piston syringes with insufficient sterility documentation. Products may not be sterile, risking infection during medical use. Affected units include specific lot numbers from 2012-2017.
Insufficient documentation to support product sterility claims.
International Medsurg is recalling 60cc piston syringes that may not be sterile, which could lead to infections if used for medical procedures. This recall affects specific batch numbers produced between 2012 and 2017.
The syringes lack sufficient documentation to prove they are sterile. This means they might not be safe for medical use, potentially causing infections if used to inject or withdraw fluids from the body.
Healthcare professionals and patients using these syringes for medical procedures are affected. Those who have the specific lot numbers listed in the recall are most at risk of infection.
Check for the catalog number SY35060LL and lot numbers starting with 12-6780-x through 15-9963-x (2012-2017). These syringes come in boxes of 50, with 8 boxes per case.
Look for the lot number on the syringe packaging, which starts with a year (e.g., 12-6780-x) and ends with -x.
The recall is due to insufficient documentation supporting that the syringes are sterile, which could lead to infections if used for medical procedures.
Check the lot number on the packaging. If it matches the listed numbers, stop using the syringes and contact International Medsurg for guidance.
Yes, the syringes may not be sterile, which could cause infections during medical procedures. This is a low-risk hazard but requires careful handling.
We’ve drafted a message you can send International Medsurg to request your refund or repair — edit it as you like.
Subject: Recall Z-2861-2017 — International Medsurg International Medsurg Hello, I own a International Medsurg that is covered by recall Z-2861-2017 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
