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

Recall Z-0654-2013 — Lockheed Martin Gyrocam Systems ( LMGS) LMGS 15" camera systems. Laser pointer and illuminator used for law enforcement surveillance from aircraft. Models DNV, TS and DS

U.S. FDA — Device Enforcement · United States · 2010-01-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0654-2013
Date of alert
2010-01-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Lockheed Martin Gyrocam Systems, Inc.
Product category
device
Product type
Devices
Reported risk: These camera systems were manufactured by LMGS and found to fail to comply with the FDA laser performance standard during an FDA inspection. These camera systems incorporate Class IIIb surveying, leveling, and alignment lasers and were entered into US commerce without a variance. Additionally, the manufacturer did not submit a product report to FDA for the camera system.
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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