SERFAS 90 degree Energy Probe — Class II medical device recall Z-1831-2015
Terminated recall by Stryker Endoscopy, reported 2015-07-01, distributed nationwide. Stryker Endoscopy is recalling all non expired SERFAS 90 degree Energy Probes due to reports of fragments of t
| Recall number | Z-1831-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Endoscopy, San Jose, CA, United States |
| Recall initiated | 2015-06-03 |
| Classified | 2015-06-24 |
| Reported by FDA | 2015-07-01 |
| Terminated | 2016-02-10 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AU, BO, BR, CH, CL, CN, CO, ES, GB, HK, IN, IT, JP, KR, MY, NL, PL, RO, SE, SG, ZA |
| Quantity | 22,063 devices |
| Lot numbers | 13128AE2 |
| Model numbers | 279-350-101 |
Product
SERFAS 90 degree Energy Probe, Part Number 279-350-101; SERFAS Energy Probes are indicated for arthroscopic procedures of the knee, shoulder, ankle, hip, elbow and wrist. Specifically, the probes are used for resection, ablation and coagulation of soft tissue, as well as the hemostasis of blood vessels.
Reason for recall
Stryker Endoscopy is recalling all non expired SERFAS 90 degree Energy Probes due to reports of fragments of the probe breaking off into the patient.
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-1831-2015. 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.