Recall of 5,000 Yale Disp 21G x 1.5in needles due to insufficient sterility documentation. Affected lots from 2012-2017; check product details to determine if recalled.
Insufficient documentation to support product sterility claims.
Yale Disp 21-gauge hypodermic needles are being recalled because the manufacturer couldn't prove they're sterile. This means some needles might not be sterile, which could lead to infections if used for medical procedures.
The needles were not properly tested for sterility, so they might contain bacteria or other contaminants. If used on a person, this could cause infections or other health issues.
Medical professionals and patients who use these needles for injections or blood draws. Those with the specific lot numbers listed are most at risk.
Check the product label for the brand 'Yale Disp', model '21 G X 1.5 in', and lot numbers starting with 12-6780-x through 15-9963-x. These needles come in boxes of 100, with 50 boxes per case.
Look for the lot numbers listed in the recall notice to determine if your needles are affected.
The manufacturer couldn't provide enough evidence that the needles are sterile, which could lead to infections if used improperly.
Check the product label for the lot numbers starting with 12-6780-x through 15-9963-x, as these are the affected batches.
The recall doesn't require discarding the needles; you only need to check if your lot numbers are affected.
We’ve drafted a message you can send Yale Disp to request your refund or repair — edit it as you like.
Subject: Recall Z-2813-2017 — Yale Disp Yale Disp Hello, I own a Yale Disp that is covered by recall Z-2813-2017 from Yale Disp. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.