Data Foundry

Medical device recalls 2014

Shaver Handpiece Sterilization Tray — Class II medical device recall Z-1872-2014

Terminated recall by Stryker Endoscopy, reported 2014-07-02. STERRAD 100S parameters provided in the Shaver Handpiece reprocessing guide (P10299 Revision A) did not fully

Recall numberZ-1872-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmStryker Endoscopy, San Jose, CA, United States
Recall initiated2014-05-19
Classified2014-06-25
Reported by FDA2014-07-02
Terminated2015-05-07
Quantity1,992 trays
Lot numbers05J034834, 06CON05774, 06CON06360, 06CON06846, 06CON06869, 06CON06960, 06CON08587, 20476.1, 23541, 23837, 25067-1-12, 26403, 26404, 26405, 26676, 26882-1-1, 26882-1-11, 26882-1-12, 26882-1-13, 26882-1-14, 27009, 27518, 28341, 30248, 34355, 35200-1-1, 35932, 36610-1-1, 36756, 38820-1-1, 39078-1-1, 39705, 40504-2-1, 40675-1-1, 41231-1-1, 41827-1-1, 42085-1-1, 42375-1-1, 42527-1-1, 42789-1-1 and 33 more
Model numbers272-700-000

Product

Shaver Handpiece Sterilization Tray. Model number 272-700-000. For sterilization of Stryker Endoscopy arthroscopic shaver.

Reason for recall

STERRAD 100S parameters provided in the Shaver Handpiece reprocessing guide (P10299 Revision A) did not fully consider all worst-case scenarios during validation testing.

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-1872-2014. 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.