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

Recall Z-2247-2021 — TJM6008 Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow Acquisition Cradle. 8G x 15 cm; TJC3513 Jamshidi" Bone Marrow Biopsy/Aspiration Needle. 13G x 8.9 cm; TJM4011 Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow Acquisition Cradle. 11G x 10cm; TJC4011 Jamshidi"

U.S. FDA — Device Enforcement · United States · 2021-06-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2247-2021
Date of alert
2021-06-23
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Bard Peripheral Vascular Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10885403044595
Reported risk: Due to complaints received regarding incomplete/open packaging seals potentially causing product to non-sterile.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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