GE Healthcare — Class II medical device recall Z-2123-2015
Terminated recall by GE Healthcare, reported 2015-07-29, distributed nationwide. A reported incident of a monitor that fell from the suspension. A fall of a monitor could result in an injury
| Recall number | Z-2123-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, Waukesha, WI, United States |
| Recall initiated | 2015-06-12 |
| Classified | 2015-07-20 |
| Reported by FDA | 2015-07-29 |
| Terminated | 2017-08-03 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BG, CA, CL, DE, DO, ES, GB, IE, IT, KW, LB, PT, RO, RU, SA, SK, TR, TW, VE |
| Serial numbers | 00000000687MC4, 00000000921MC7, 00000000952MC2, 00000001055MC3, 00000001057MC9, 00000001101MC5, 00000001275MC7, 00000001286MC4, 00000001302MC9, 00000001333MC4, 00000001343MC3, 00000001406MC8, 00000001408MC4, 00000001415MC9, 00000001419MC1, 00000001420MC9, 00000001430MC8, 00000001452MC2, 00000001459MC7, 00000001505MC7, 00000001658MC4, 00000001746MC7, 00000001889MC5, 00000002207MC9, 00000003511MC3 and 18 more |
Product
GE Healthcare, Precision MPi fluoroscopic imaging systems.
Reason for recall
A reported incident of a monitor that fell from the suspension. A fall of a monitor could result in an injury to a patient or operator. Recall affects the single and dual LCD monitor suspensions used on Precision 500D Classical R & F system, Precision RXi 23A/32A Analog System, Precision RXi Digital system and Precision MPi fluoroscopic imaging systems.
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-2123-2015. 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.