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

Recall Z-1555-2014 — Nonabsorbable Surgical Suture, U.S.P., Sterile - Do Not Resterilize, Deknatel. Indicated for use in soft tissue approximation.

U.S. FDA — Device Enforcement · United States · 2014-03-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1555-2014
Date of alert
2014-03-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Teleflex Medical
Product category
device
Product type
Devices
Reported risk: Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use.
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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