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

Recall Z-1684-2015 — CODMAN 3000 Series Refill Set- Huber needles. Used in combination with the CODMAN 3000 Series Constant Flow Implantable Pump CATALOG NO. : AP-07014 Each CODMAN 3000 Refill Kit contains 2 (two) 22 Gauge x 1.5 Huber Point Needles which are used in conjunction with a 50 mL Calibrated Syringe Barrel

U.S. FDA — Device Enforcement · United States · 2015-03-05 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1684-2015
Date of alert: 2015-03-05
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Codman & Shurtleff, Inc.
Product category: device
Product type: Devices

Reported risk: Needle is leaking from hub/needle cannula connection

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.

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