RecallRadar

FDA Device recall Z-1881-2025

Segmental Stem, Canal Filling, Straight, 120MM, 1 EACH. Model Numbers: FS-11120-03M, FS-12120-03M, FS-13120-03M, FS-14120-03M, FS-15120-03M…

On 2025-06-04 the FDA classified a Class II recall of Segmental Stem, Canal Filling, Straight, 120MM, 1 EACH. Model Numbers: FS-11120-03M, FS-12120-03M, FS-13120-03M, FS-14120-03M, FS-15120-03M… by Onkos Surgical, citing potential for breach of Tyvek seals.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1881-2025
ClassificationClass II
Statusongoing
Initiated2023-09-01
Published2025-06-04
Last updated2026-09-13 11:57 UTC
CompanyOnkos Surgical
DistributionAZ, FL, GA, HI, IL, KS, KY, LA, MD, MS, NC, NE, NJ, OH, PA, TX, WA, WI

Product

Segmental Stem, Canal Filling, Straight, 120MM, 1 EACH. Model Numbers: FS-11120-03M, FS-12120-03M, FS-13120-03M, FS-14120-03M, FS-15120-03M, FS-16120-03M, FS-17120-03M, FS-18120-03M, FS-19120-03M, FS-20120-03M, FS-21120-03M. Component of ELEOS LIMB SALVAGE SYSTEM

Reason

Potential for breach of Tyvek seals.

Identifiers

code_info
a. Model Number: FS-11120-03M; UDI-DI: B278FS1112003M0; Lot Numbers: 1880532, 1880533, 1880534, 1880535, 1880536, 18805…a. Model Number: FS-11120-03M; UDI-DI: B278FS1112003M0; Lot Numbers: 1880532, 1880533, 1880534, 1880535, 1880536, 1880537, 1880538, 1880539, 1880540, 1880541, 1880542, 1880543. b. Model Number: FS-12120-03M; UDI-DI: B278FS1212003M0; Lot Numbers: 1880544, 1880545, 1880546, 1880547, 1880548, 1880549, 1880550, 1880551, 1880552, 1880553. c. Model Number: FS-13120-03M; UDI-DI: B278FS1312003M0; Lot Numbers: 1880554, 1880555, 1880556, 1880557, 1880558, 1880559, 1880560, 1880561, 1880562, 1880563. d. Model Number: FS-14120-03M; UDI-DI: B278FS1412003M0; Lot Numbers: 1880564, 1880565, 1880566, 1880567, 1880568, 1880569, 1880570, 1880571, 1880572, 1880573, 1880574. e. Model Number: FS-15120-03M; UDI-DI: B278FS1512003M0; Lot Numbers: 1880575, 1880576, 1880577, 1880578, 1880579, 1880580, 1880581, 1880582, 1880583, 1880584, 1880585, 1880586, 1880587. f. Model Number: FS-16120-03M; UDI-DI: B278FS1612003M0; Lot Numbers: 1880588, 1880589, 1880590, 1880591, 1880592, 1880593, 1880594, 1880595, 18805

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1881-2025%22

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