Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
T-Lok Bone Marrow Biopsy Needle 8G x 4 Ext Can 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
T-Lok Bone Marrow Biopsy Needle 8G x 4 Ext Can, Part Number DBMNJ0804TL; T-Lok Bone Marrow Biopsy Needle 11G x 4 Ext Can, Part Number DBMNJ1104TL; Bone Marrow Biopsy Needle 13G x 4, Part Number DBMNJ1304
Quantity: 10290 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