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

Recall Z-1196-2017 — HARVEST NEEDLE 15GA X 2 Intended for the purpose of harvesting bone and/or bone marrow specimens

U.S. FDA — Device Enforcement · United States · 2017-01-18 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1196-2017
Date of alert
2017-01-18
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)
11158857
Reported risk: The recalling firm received a complaint from one of their customers of a 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

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.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.