RecallRadar

FDA Device recall Z-0654-2013

Lockheed Martin Gyrocam Systems ( LMGS) LMGS 15" camera systems

On 2013-02-20 the FDA classified a Class II recall of Lockheed Martin Gyrocam Systems ( LMGS) LMGS 15" camera systems by Lockheed Martin Gyrocam Systems, citing 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….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0654-2013
ClassificationClass II
Statusterminated
Initiated2010-01-21
Published2013-02-20
Last updated2026-09-13 11:53 UTC
CompanyLockheed Martin Gyrocam Systems
DistributionUS

Product

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

Reason

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.

Identifiers

code_info
Gyrocam DNV Camera System, Serial Numbers: 137, 138, 141, 142, 143, 144, 145, 148, 150, 151, 152, 158, 159, 160, 164,…Gyrocam DNV Camera System, Serial Numbers: 137, 138, 141, 142, 143, 144, 145, 148, 150, 151, 152, 158, 159, 160, 164, 165, 170, 172, 173, 174, 175, 177; Gyrocam DS Camera System, Serial Numbers: 134, 140, 147, 153, 169, 181; Gyrocam TS Camera System, Serial Numbers: 132, 146, 149, 171, 502.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0654-2013%22

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