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

Recall Z-2940-2020 — Medcomp 15.SF X 24CM Titan HD CATHETER (CUFF 19CM FROM TIP) Ref: THD155024

U.S. FDA — Device Enforcement · United States · 2020-07-27 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2940-2020
Date of alert
2020-07-27
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medical Components, Inc dba MedComp
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
884908129304
Reported risk: Kits were packaged with the incorrect size valve peelable introducer. The kits include a 15F instead of the correct 16F valve peelable introducer
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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