Recalled BD Yale 19G x 1.5in hypodermic needles due to insufficient sterility documentation. Check product details to determine if affected.
Insufficient documentation to support product sterility claims.
International Medsurg Connection, Inc. is recalling BD Yale 19G x 1.5in hypodermic needles because the product's sterility claims lack sufficient documentation. This could lead to potential contamination risks during medical procedures.
The needles were manufactured without adequate documentation to prove they meet sterility standards. This could result in contaminated needles being used, potentially causing infections during medical procedures.
Medical professionals and patients using these needles for injections or fluid withdrawal. Those with the specific lot numbers listed in the recall are most at risk.
Check for the product name 'BD Yale DISP RG', 19G x 1.5in needles, 100 per box, 50 boxes per case. Affected lots include specific numbers starting with 12-6780-x through 17-1791-x.
Identify the lot numbers listed in the recall to determine if your needles are affected.
The needles lack sufficient documentation to support their sterility claims, which could lead to contamination risks during medical procedures.
Look for the product name 'BD Yale DISP RG', 19G x 1.5in needles, 100 per box, 50 boxes per case. Affected lots include specific numbers starting with 12-6780-x through 17-1791-x.
Check the lot numbers against the list provided in the recall to determine if your needles are affected. If affected, contact the manufacturer for further instructions.
We’ve drafted a message you can send BD Yale to request your refund or repair — edit it as you like.
Subject: Recall Z-2809-2017 — BD Yale BD Yale Hello, I own a BD Yale that is covered by recall Z-2809-2017 from BD Yale. 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.
