International Medsurg recalls 20cc piston syringes with insufficient sterility documentation. Products may not be sterile, posing infection risks. Check catalog numbers and known lots for affected items.
Insufficient documentation to support product sterility claims.
International Medsurg is recalling 20cc piston syringes due to insufficient documentation supporting their sterility claims. This means the syringes might not be sterile, which could lead to infections if used for medical procedures.
The syringes lack proper documentation to confirm they are sterile. This could mean the syringes might contain contaminants, leading to infections when used for medical procedures.
Patients using these syringes for medical procedures or injections are at risk of infection if the syringes are not sterile. Healthcare providers and individuals with medical conditions requiring injections may be affected.
Check for catalog number SY35020LS and known lot numbers listed in the recall (e.g., 12-6780-x, 12-6925-x, etc.). These syringes were sold in boxes of 100, with 9 boxes per case.
Look for the catalog number SY35020LS and known lot numbers listed in the recall to confirm if your syringes are affected.
The recall is due to insufficient documentation supporting sterility claims, which means the syringes might not be sterile and could lead to infections.
Check the catalog number and known lot numbers to see if your syringes are affected. If they are, you may need to contact the manufacturer for guidance.
Yes, the syringes might not be sterile, which could cause infections if used for medical procedures.
We’ve drafted a message you can send International Medsurg to request your refund or repair — edit it as you like.
Subject: Recall Z-2858-2017 — International Medsurg International Medsurg Hello, I own a International Medsurg that is covered by recall Z-2858-2017 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.
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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.
