Bard recalls 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needles (REF TIN3015) with potential for needle protector to dislodge, causing needle stick injuries.
Potential for needle protector to become fully dislodge exposing infusion needle which could result in needle stick.
Bard is recalling certain bone marrow aspiration needles due to a risk that the needle protector may become fully dislodged, exposing the needle and potentially causing a needle stick injury. This could lead to infection or other complications for medical users.
The needle protector may become fully dislodged during use, exposing the sharp needle. This could result in a needle stick injury to the user or patient, potentially leading to infection or other complications.
Healthcare professionals and medical facilities using the recalled needles are most at risk. Patients receiving procedures with these needles could also be affected.
Check for the product name 'Bone Marrow Aspiration/Intraosseous Infusion Needle' with the model REF TIN3015. The lot/serial numbers listed in the recall record indicate specific batches produced between 2021 and 2026.
Immediately stop using any recalled needles with the model REF TIN3015 and the listed lot/serial numbers.
The recalled model is REF TIN3015, a 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle.
Check the lot/serial numbers on your needle against the list provided in the recall record, which includes specific batches from 2021 through 2026.
The recall record does not specify a return process, but you should stop using the recalled needles immediately.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-0002-2022 — Bard Bard Hello, I own a Bard that is covered by recall Z-0002-2022 from Bard. 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.
