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Terminated

Dr. Fog Endoscopic fog prevention kit.

FDA Recall Z-0897-05 · Posted 2005-06-16

Recalling FirmAspen Surgical Products, Inc.
Recall StatusTerminated
Product CodeKOG
Date Initiated2005-05-15
Date Terminated2005-09-16
Product Quantity2460 packages.

Reason for Recall

An improper expiration date was placed on the individual packages, although the dispenser box and carton contained the correct expiration date.

Firm Action

Consignees were notified via phone on 5/15/05. Wholesalers were requested to notify their customers.

Root Cause

Process control

Distribution Pattern

Nationwide.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K932449DR. FOGO.R. Concepts, Inc. · 1993-08-11

Official Source

View FDA Recall →

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

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