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Terminated

Multi Absorbers, reference number 8003138, in S/5 Aespire Start-up Kits (each containing 2 Multi Absorbers)

FDA Recall Z-0714-03 · Posted 2003-04-09

Recalling FirmDatex-Ohmeda
Recall StatusTerminated
Product CodeBSF
Date Initiated2003-02-12
Date Terminated2004-07-02
Product Quantity5 S/5 Aespire Start-up kits

Reason for Recall

Multi Absorbers for anesthesia delivery equipment may have missing or damaged filters, exposing the patient to dust from soda lime in the absorbers.

Firm Action

Recall letters dated February 12, 2003 requested that the product be removed from use and returned.

Root Cause

Other

Distribution Pattern

Nationwide in the United States.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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