International Medsurg recalls 30cc piston syringes with insufficient sterility documentation. Products may not be sterile, posing infection risks during medical use. Affected units include specific lot numbers from 2012-2017.
Insufficient documentation to support product sterility claims.
International Medsurg is recalling 30cc piston syringes that lack proper sterility documentation. This means the syringes might not be sterile, which could lead to infections if used for medical procedures. Affected units have specific lot numbers from 2012 to 2017.
The syringes were not properly documented as sterile, which means they might not meet safety standards for medical use. If used without proper sterility, they could introduce infections into the body during medical procedures.
Patients using these syringes for medical procedures, such as injections or fluid withdrawal, are at risk of infection if the syringes are not sterile. Healthcare providers and individuals with medical conditions requiring such syringes are most affected.
Check for the catalog number SY35030LS and lot numbers starting with 12-6780-x through 15-9963-x (2012-2017). These syringes come in boxes of 50, with 9 boxes per case (450 total per case).
Look for the catalog number SY35030LS and lot numbers listed in the recall notice to confirm if your syringes are affected.
The recall is due to insufficient documentation supporting that the syringes are sterile, which could lead to infection risks during medical use.
Check the catalog number and lot numbers to see if your syringes are affected. If they are, you should stop using them to avoid infection risks.
Yes, affected lot numbers range from 12-6780-x through 15-9963-x (2012-2017). Check your syringes against this list.
We’ve drafted a message you can send International Medsurg to request your refund or repair — edit it as you like.
Subject: Recall Z-2860-2017 — International Medsurg International Medsurg Hello, I own a International Medsurg that is covered by recall Z-2860-2017 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.
