Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2189-2015 — 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

U.S. FDA — Device Enforcement · United States · 2015-06-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2189-2015
Date of alert
2015-06-18
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Argon Medical Devices, Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
11088295
Reported risk: Potential defect in the forming of the primary package of the blister that may compromise the sterility of the product inside the tray.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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