Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bone Marrow Aspiration Needle 15G x 2.688 MAX Recalled by Argon Medical Devices, Inc Due to Potential defect in the forming of the primary...
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 Argon Medical Devices, Inc directly.
Affected Products
Bone Marrow Aspiration Needle 15G x 2.688 MAX, Part Number DBMNI1501; Bone Marrow Aspiration Needle 15G x 4 MAX, Part Number DBMNI1504; Bone Marrow Aspiration Needle 16G x 2.688 MAX, Part Number DBMNI1601
Quantity: 6390 units
Why Was This Recalled?
Potential defect in the forming of the primary package of the blister that may compromise the sterility of the product inside the tray.
Where Was This Sold?
US
About Argon Medical Devices, Inc
Argon Medical Devices, Inc has 42 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report