Lockheed Martin Gyrocam Systems — Class II medical device recall Z-0654-2013
Terminated recall by Lockheed Martin Gyrocam Systems, Inc., reported 2013-02-20, distributed nationwide. These camera systems were manufactured by LMGS and found to fail to comply with the FDA laser performance stan
| Recall number | Z-0654-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Lockheed Martin Gyrocam Systems, Inc., Sarasota, FL, United States |
| Recall initiated | 2010-01-21 |
| Classified | 2013-02-14 |
| Reported by FDA | 2013-02-20 |
| Terminated | 2015-02-24 |
| Distributed | Nationwide (US) |
| Quantity | 33 units |
| Serial numbers | 132, 134, 137, 138, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 158, 159, 160, 164, 165, 169, 170 and 8 more |
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 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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0654-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.