Recalled piston syringes and needles may not meet sterility standards. Check product details to determine if affected. Contact manufacturer for guidance.
Insufficient documentation to support product sterility claims.
International Medsurg Connection is recalling piston syringes and hypodermic needles that lack sufficient documentation to prove they are sterile. This could lead to infections if used improperly.
The syringes and needles were not properly documented as sterile, which could result in contamination and infection if used in medical procedures. This is a documentation issue rather than a physical defect.
Healthcare professionals and individuals using these medical devices for injections or fluid withdrawal. Those with the specific product model and lot numbers listed are most at risk.
Check for the product model: Piston Syringe and Hypodermic Needle, 3 CC L/L 25 G X 5/8, 100 per box, 24 boxes/case. Look for lot numbers starting with 12-6780-x through 15-9963-x as listed in the recall.
Identify the product model and lot numbers to confirm if it is affected by this recall.
The recall is due to insufficient documentation supporting the product's sterility claims, which could lead to contamination and infection if used improperly.
The official recall notice does not specify a remedy, so contact International Medsurg Connection directly for guidance.
Yes, the affected lot numbers range from 12-6780-x through 15-9963-x as listed in the recall notice.
We’ve drafted a message you can send International Medsurg Connection to request your refund or repair — edit it as you like.
Subject: Recall Z-2837-201 — International Medsurg Connection International Medsurg Connection Hello, I own a International Medsurg Connection that is covered by recall Z-2837-201 from International Medsurg Connection. 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.
