Recall of 1,000-unit cases of piston syringes and needles due to lack of sterility documentation. Affected products may not be safe for medical use.
Insufficient documentation to support product sterility claims.
International Medsurg is recalling piston syringes and hypodermic needles that lack proper sterility documentation. This could mean the products are not safe for medical use, potentially leading to infections or other health risks.
The products were not properly documented as sterile, which means they might not be safe for medical use. This could lead to infections or other health issues if used improperly.
Healthcare professionals and individuals using these products for medical procedures are affected. Those who have the specific model numbers listed in the recall are at risk.
Check for the product model: Piston Syringe and Hypodermic Needle, 10 CC L/L 20 G X 1.5, 100 per box, 10 boxes/case, 1,000/case. Look for known lot numbers starting with 12-6780-x through 16-1165-x.
Identify the specific product model and lot numbers listed in the recall to confirm if your items are affected.
The products lack sufficient documentation to support sterility claims, which could mean they are not safe for medical use.
Check the product model and lot numbers against the list provided in the recall to see if they are affected. If they are, you should stop using them and contact the manufacturer.
Yes, the recall includes lot numbers starting with 12-6780-x through 16-1165-x. Check your product's lot number to see if it matches.
We’ve drafted a message you can send International Medsurg to request your refund or repair — edit it as you like.
Subject: Recall Z-2845-2017 — International Medsurg International Medsurg Hello, I own a International Medsurg that is covered by recall Z-2845-2017 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.
