Mavig Monitor Suspension System — Class II medical device recall Z-0763-2016
Terminated recall by GE Medical Systems, LLC, reported 2016-02-17, distributed nationwide. GE Healthcare has recently become aware of a reported incident in which a Mavig suspension arm with monitor as
| Recall number | Z-0763-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Medical Systems, LLC, Waukesha, WI, United States |
| Recall initiated | 2015-12-18 |
| Classified | 2016-02-05 |
| Reported by FDA | 2016-02-17 |
| Terminated | 2016-09-07 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, AU, BE, BG, BH, BR, CA, CH, CN, CO, CZ, DE, DK, DO, DZ, EC, EG, ES, FI, FR, GB, GR, GT, HK, HR, HU, ID, IE, IL, IN, IQ, IR, IS, IT, JO, JP, KR, KW, LB, LT, LV, MA, MX, MY, NG, NL, NO, NZ, PA, PH, PK, PL, PT, RO, RS, RU, SA, SE, SG, SI, SK, TH, TN, TR, TW, UY, VE, ZA |
| UPC / GTIN / UDI-DI | 00082406090014, 00082416040023, 00082416070006, 00082416100017, 00082416120008, 00082416120015, 00082416130021, 00082416140006, 00082416160004, 00082416160011, 00082416190001, 00082416200007, 00082416210006, 00082416210013, 00082416310003, 00082416310010, 03178183100200, 03178183100910, 08301686210076 |
| Model numbers | GD60 |
Product
Mavig Monitor Suspension System, Model GD60, contained in the following Fluoroscopic imaging systems: Advantx LCV+, Advantx LCN+, Advantx LCLP+, Advantx LCA, INNOVA 2000, INNOVA 4100, INNOVA 3100, INNOVA 3131IQ, INNOVA 2121IQ, INNOVA 2100IQ, INNOVA 3100IQ, and INNOVA 4100IQ
Reason for recall
GE Healthcare has recently become aware of a reported incident in which a Mavig suspension arm with monitor assembly fell to the floor.
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-0763-2016. 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.