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

Recall Z-0087-2018 — RX-2 COUDE Epidural Needle, 16g x 3.5in (8.9cm)TW, 10 units, Calibrated, Plastic Hub, Detachable Wing, Blunt Stylet, Sterile, Rx only, For Use with 19g or Smaller Catheter

U.S. FDA — Device Enforcement · United States · 2017-07-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0087-2018
Date of alert
2017-07-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Epimed International
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
12168200
Reported risk: Potential for partially incomplete seal of product, impacting sterility.
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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