Recalled piston syringes and needles due to lack of sterility documentation. Check product details to determine if affected.
Insufficient documentation to support product sterility claims.
International Medsurg is recalling piston syringes and hypodermic needles that lack proper sterility documentation. This could lead to infections if used for medical procedures.
The products were not properly documented as sterile, which could result in contamination and infection if used for injections or blood draws. This is a critical issue for medical devices.
Healthcare professionals and patients using these syringes for medical procedures. Those with the specific lot numbers listed are most at risk.
Check for the product model: 5 CC L/L 22 G X 1.5, 100 per box, 15 boxes per 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 recalled.
The products lack sufficient documentation to support sterility claims, which could lead to infections if used for medical procedures.
Check the product details and lot numbers to see if it is affected; the recall does not provide a specific remedy.
Yes, the lack of sterility documentation could result in contamination and infection 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-2843-2017 — International Medsurg International Medsurg Hello, I own a International Medsurg that is covered by recall Z-2843-2017 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.
