Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
REF TIN3015 Recalled by Bard Peripheral Vascular Inc Due to Potential for needle protector to become fully dislodge...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Bard Peripheral Vascular Inc directly.
Affected Products
REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796
Why Was This Recalled?
Potential for needle protector to become fully dislodge exposing infusion needle which could result in needle stick.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bard Peripheral Vascular Inc
Bard Peripheral Vascular Inc has 136 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report