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

Recall Z-0649-2013 — Sterile Rigid Tip Suction Wand The Suction Wands are indicated for use to remove excess fluid from the surgical field.

U.S. FDA — Device Enforcement · United States · 2012-11-02 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0649-2013
Date of alert
2012-11-02
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
California Medical Laboratories Inc
Product category
device
Product type
Devices
Reported risk: California Medical Laboratories, Inc. has identified an issue with the Rigid Tip Suction Wand. Due to insufficient adhesive application, the distal tip has the potential to come loose from the wand and fall into the patient's chest cavity.
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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