Data Foundry

Medical device recalls 2025

Segmental Stem — Class II medical device recall Z-1880-2025

Ongoing recall by Onkos Surgical, Inc., reported 2025-06-04, distributed in AZ, FL, GA, HI, IL, KS, KY, LA…. Potential for breach of Tyvek seals.

Recall numberZ-1880-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmOnkos Surgical, Inc., Parsippany, NJ, United States
Recall initiated2023-09-01
Classified2025-05-29
Reported by FDA2025-06-04
DistributedAZ, FL, GA, HI, IL, KS, KY, LA, MD, MS, NC, NE, NJ, OH, PA, TX, WA, WI
Quantity49 units
Lot numbers1880259, 1880260, 1880261, 1880262, 1880263, 1880264, 1880265, 1880266, 1880267, 1880268, 1880269, 1880270, 1880271, 1880272, 1880273, 1880274, 1880275, 1880276, 1880277, 1880278, 1880279, 1880280, 1880281, 1880282, 1880283, 1880284, 1880285, 1880286, 1880287, 1880288, 1880289, 1880290, 1880291, 1880292, 1880293, 1880294, 1880295, 1880296, 1880297, 1880298 and 9 more
Model numbersCB-11152-03M, CB-13152-03M, CB-15152-03M, CB-17152-03M

Product

Segmental Stem, Cemented, Bowed, 152MM, 1 EACH. Model Numbers: CB-11152-03M, CB-13152-03M, CB-15152-03M, CB-17152-03M. Component of ELEOS LIMB SALVAGE SYSTEM

Reason for recall

Potential for breach of Tyvek seals.

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-1880-2025. 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.