Recalled piston syringes and hypodermic needles due to insufficient documentation supporting sterility claims. Affected units include specific lot numbers and quantities.
Insufficient documentation to support product sterility claims.
International Medsurg Connection is recalling piston syringes and hypodermic needles that lack proper sterility documentation. This could lead to contamination risks if used for medical procedures.
The products do not have sufficient documentation to confirm they are sterile. This means there is a potential risk of contamination if used for medical procedures, which could lead to infections or other complications.
Medical professionals and individuals using these syringes for injections or fluid withdrawal may be affected. Those with the specific lot numbers listed are at risk.
Check for the product name 'Piston Syringe and Hypodermic Needle, 3 CC L/L 22 G X 1.25, 100 per box' with the listed lot numbers (e.g., 12-6780-x, 12-6925-x).
Identify if your syringes have the specific lot numbers listed in the recall notice.
The products lack sufficient documentation to support sterility claims, which could lead to contamination risks during medical procedures.
Check the lot numbers on your syringes against the list provided in the recall notice. If they match, stop using them and contact the manufacturer for further instructions.
Yes, the recall includes specific lot numbers starting with '12-' through '17-' followed by 'x' (e.g., 12-6780-x, 13-7538-x).
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-2833-2017 — International Medsurg Connection International Medsurg Connection Hello, I own a International Medsurg Connection that is covered by recall Z-2833-2017 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.
