Philips Healthcare SureSigns VS2+ Model 863278 SureSigns VS2+ NBP and… — Class II medical device recall Z-0824-2013
Terminated recall by Philips Healthcare Inc., reported 2013-02-20, distributed nationwide. VS2+ screen may lock up and stop monitoring during patient use
| Recall number | Z-0824-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Healthcare Inc., Andover, MA, United States |
| Recall initiated | 2013-01-14 |
| Classified | 2013-02-14 |
| Reported by FDA | 2013-02-20 |
| Terminated | 2020-08-27 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BE, CA, CH, CL, DE, DK, ES, FR, GB, IE, IL, IN, IS, IT, JO, KE, KR, KW, LB, MY, NL, NO, NZ, PL, PT, SA, SE, SG, SI, TH, TT, ZA |
| Quantity | 3,248 units |
| Serial numbers | CN14800101, CN14800102, CN14800103, CN14800104, CN14800105, CN14800106, CN14800107, CN14800108, CN14800109, CN14800110, CN14800111, CN14800112, CN14800113, CN14800114, CN14800115, CN14800116, CN14800117, CN14800118, CN14800119, CN14800120, CN14800121, CN14800122, CN14800123, CN14800124, CN14800125 and 475 more |
| Model numbers | 863278, 863279 |
Product
Philips Healthcare SureSigns VS2+ Model 863278 SureSigns VS2+ NBP and SpO2 Model 863279 SureSigns VS2+ NBP, SpO2 and Temperature Product Usage: 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.
Reason for recall
VS2+ screen may lock up and stop monitoring during patient use
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-0824-2013. 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.