BD recalls 32G X 4mm pen needles (Lot 9044773) due to potential sterility issues after February 29, 2024 expiry. Consumers should check their product's expiry date and contact BD for guidance.
BD Nano 2nd Gen Pen Needle was shipped close to or after the labeled expiration date of February 29, 2024. Using a device past its expiry sterility and integrity of the device cannot be guaranteed.
BD is recalling 32G X 4mm pen needles that may have expired after February 29, 2024. Using expired needles risks contamination and infection. Affected users should check their product's expiry date and contact BD.
Expired needles may lose sterility and integrity, increasing infection risk during injections. The hazard occurs because the product was shipped close to or after its labeled expiration date.
Patients using BD Nano 2nd Gen Pen Needles for injections. Those with needles past the February 29, 2024 expiry date are most at risk.
Check for the lot number 9044773 and expiry date of February 29, 2024 on the needle packaging. The product is part of the Patient Counseling Sample Toolbox with catalog number 6484755.
Look for the expiry date of February 29, 2024 on the needle packaging.
Reach out to BD for guidance on next steps if your needles are past expiry.
BD recalls these needles because they were shipped close to or after the labeled expiration date of February 29, 2024, which risks sterility and integrity.
Check for lot number 9044773 and expiry date of February 29, 2024 on the needle packaging. The product is part of the Patient Counseling Sample Toolbox with catalog number 6484755.
Contact BD for guidance on next steps if your needles are past expiry.
We’ve drafted a message you can send BD to request your refund or repair — edit it as you like.
Subject: Recall Z-2424-2024 — BD BD Hello, I own a BD that is covered by recall Z-2424-2024 from BD. 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.
