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

Recall Z-1336-2019 — Tissu-Trans Syringe Fill 360, Catalog 3-TT-SFILL 360, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.

U.S. FDA — Device Enforcement · United States · 2018-02-02 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1336-2019
Date of alert
2018-02-02
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Shippert Medical Technologies
Product category
device
Product type
Devices
Reported risk: The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.
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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