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

Recall Z-0058-2021 — ClearPro Closed Suction Catheter, Model DYNCPDS14T, 14 Fr FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only.

U.S. FDA — Device Enforcement · United States · 2020-09-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0058-2021
Date of alert
2020-09-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medline Industries Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
06919010016
Reported risk: There have been reports of the suction catheter coming apart from the device assembly 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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