Recalled piston syringes and needles due to lack of sterility documentation. Affected products include specific lot numbers and quantities. Consumers should check their product details.
Insufficient documentation to support product sterility claims.
International Medsurg is recalling piston syringes and hypodermic needles because the products lack sufficient documentation to support their sterility claims. This means the products may not be sterile, which could lead to infections if used for medical procedures.
The products do not have adequate documentation proving they are sterile. This could result in infections if the syringes or needles are used for medical procedures without proper sterility.
Medical professionals and individuals using these syringes for injections or fluid withdrawal may be affected. Those with the specific lot numbers listed are most at risk.
Check for the product name 'Piston Syringe and Hypodermic Needle, 10 CC L/L 21 G X 1.0, 100 per box, 10 boxes/case, 1,000/case'. Look for lot numbers starting with 12-6780-x through 15-9963-x as listed in the recall.
Identify the product name and lot numbers to confirm if your syringes or needles are affected.
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 they are affected. If they are, you should stop using them and contact the manufacturer for further instructions.
Yes, the affected lot numbers start with 12-6780-x through 15-9963-x as listed in the recall 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-2846-2017 — International Medsurg International Medsurg Hello, I own a International Medsurg that is covered by recall Z-2846-2017 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.
