International Medsurg recalls 3cc piston syringes and needles that lack proper sterility documentation. These medical devices could pose infection risks if used without confirmed sterility.
Insufficient documentation to support product sterility claims.
International Medsurg is recalling piston syringes and hypodermic needles that may not be sterile due to insufficient documentation. Using these products could lead to infections if they are not properly sterilized.
The products lack sufficient documentation to support sterility claims. This means the syringes and needles might not be sterile, increasing the risk of infection when used for medical procedures.
Healthcare professionals and individuals using these medical devices for injections or fluid withdrawal. Those most at risk are people who have used the recalled syringes and needles for medical procedures.
Check for the product name 'Piston Syringe and Hypodermic Needle, 3 CC L/L 20 G X 1.5, 100 per box'. Look for lot numbers starting with 12-6780-x through 15-9963-x as listed in the recall.
Identify the product by checking the lot numbers listed in the recall notice.
The products lack sufficient documentation to support sterility claims, which could lead to infection risks if used without confirmed sterility.
The recall does not specify a remedy, so you should check the product details and contact the manufacturer for further guidance.
Yes, the recall includes lot numbers starting with 12-6780-x through 15-9963-x as listed in the notice.
We’ve drafted a message you can send International Medsurg to request your refund or repair — edit it as you like.
Subject: Recall Z-2829-2017 — International Medsurg International Medsurg Hello, I own a International Medsurg that is covered by recall Z-2829-2017 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.
