ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Systems — Class II medical device recall Z-0785-2014
Terminated recall by Philips Medical Systems (Cleveland) Inc, reported 2014-01-29, distributed nationwide. The recalling firm determined that visual inspections of the fork joints behind the detector that are conducte
| Recall number | Z-0785-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Medical Systems (Cleveland) Inc, Cleveland, OH, United States |
| Recall initiated | 2013-12-04 |
| Classified | 2014-01-17 |
| Reported by FDA | 2014-01-29 |
| Terminated | 2015-11-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, BE, CA, DE, DK, GB, IT, KR, NL, NO, PK, RU, SG |
| Quantity | 255 units |
| Reason classes | packaging |
| Serial numbers | 00709B, 0101003A, 01310B, 01525B, 01920B, 01921B, 01922B, 03041B, 03094B, 03338B, 03368B, 1023, 106785, 1100005, 1178, 1292, 136560, 2145-30074A, 7718B, 9051005, 9211014, 93-10678, 9301005, 9304019, 9304024 and 69 more |
| Model numbers | 882060, 88294, 88295 |
Product
ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Systems. Distributed by Philips Medical Systems, Cleveland, OH
Reason for recall
The recalling firm determined that visual inspections of the fork joints behind the detector that are conducted during six month preventive maintenance (PM) may not detect small cracks or deficiencies in the fork weldment.
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-0785-2014. 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.