Philips SureSigns VSi/VS2+ patient monitors Model Part Numbers VSi/… — Class II medical device recall Z-2303-2012
Terminated recall by Philips Healthcare Inc., reported 2012-09-05, distributed nationwide. Philips SureSigns VSi/VS2+ patient monitors may not be properly secured and may fall from the wall mount
| Recall number | Z-2303-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Healthcare Inc., Andover, MA, United States |
| Recall initiated | 2012-08-15 |
| Classified | 2012-08-30 |
| Reported by FDA | 2012-09-05 |
| Terminated | 2014-03-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BE, BH, CH, DE, DK, ES, FR, GB, IE, IL, IN, IS, IT, JO, KE, LB, MY, NL, NO, PL, PT, SA, SE, SI, SV, ZA |
| Quantity | 2,314 units |
| Model numbers | 863275, 863276, 863277, 863278, 863279 |
Product
Philips SureSigns VSi/VS2+ patient monitors Model Part Numbers VSi/ 863275, 863276, 863277, VS2+ 863278, 863279. The SureSigns VS2+ vital signs monitor is for monitoring, recording and alarming of multiple physiological parameters of adults, pediatrics, and neonates in healthcare environments. Additionally, the monitor is intended for use in transport situations within a healthcare facility. The SureSigns VSi vital signs monitor is for measurement of multiple physiological parameters of adults, pediatrics, and neonates in healthcare environments. Additionally, the monitor is intended for use in transport situations within a healthcare facility
Reason for recall
Philips SureSigns VSi/VS2+ patient monitors may not be properly secured and may fall from the wall mount
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-2303-2012. 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.