CLASS II Device recall · Reported 20 Feb 2013 · FDA Enforcement Report
( Lmgs) Lmgs 15" camera systems recalled by Lockheed Martin Gyrocam
Lockheed Martin Gyrocam Systems is recalling Lockheed Martin Gyrocam Systems ( Lmgs) Lmgs 15" camera systems, distributed nationwide in the US. The recall was initiated on 21 Jan 2010 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0654-2013
- FDA event ID
- 64029
- Recalling firm
- Lockheed Martin Gyrocam Systems, Sarasota, FL
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 21 Jan 2010
- FDA classified
- 14 Feb 2013
- Reported
- 20 Feb 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Processing Deviation
- Device type
- Other Medical Devices
Timeline
| 21 Jan 2010 | Recall initiated by company | |
| 14 Feb 2013 | Classified by FDA | +1120 days |
| 20 Feb 2013 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
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.
The USDA issues these when meat or poultry was produced without proper inspection, or when a step such as cooking or pasteurisation did not meet requirements.
Product as listed by the FDA
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
Where it was distributed
Nationwide Distribution
Questions about this recall
Is ( Lmgs) Lmgs 15" camera systems recalled?
Yes. Lockheed Martin Gyrocam Systems recalled ( Lmgs) Lmgs 15" camera systems on 21 Jan 2010. The recall is Class II and its status is Terminated. Recall number Z-0654-2013.
Why was it recalled?
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.
Which lots are affected?
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.
Where was it sold?
Nationwide Distribution
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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