FDA Device recall Z-1883-2025

Ethos Collar Stem, Cemented, Fluted, 100MM, 1 EACH. Model Numbers: HC-09100-03M, HC-10100-03M, HC-11120-03M, HC-13120-03M, HC-15120-03M, HC…

FDA Device
Class II
ongoing
Published 2025-06-04

On 2025-06-04 the FDA classified a Class II recall of Ethos Collar Stem, Cemented, Fluted, 100MM, 1 EACH. Model Numbers: HC-09100-03M, HC-10100-03M, HC-11120-03M, HC-13120-03M, HC-15120-03M, HC… by Onkos Surgical, citing potential for breach of Tyvek seals.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1883-2025
Classification	Class II
Status	ongoing
Initiated	2023-09-01
Published	2025-06-04
Last updated	2026-09-13 11:57 UTC
Company	Onkos Surgical
Distribution	AZ, FL, GA, HI, IL, KS, KY, LA, MD, MS, NC, NE, NJ, OH, PA, TX, WA, WI

Product

Ethos Collar Stem, Cemented, Fluted, 100MM, 1 EACH. Model Numbers: HC-09100-03M, HC-10100-03M, HC-11120-03M, HC-13120-03M, HC-15120-03M, HC-17120-03M. Component of ELEOS SEGMENTAL LIMB SALVAGE SYSTEM

Reason

Potential for breach of Tyvek seals.

Identifiers

code_info	a. Model Number: HC-09100-03M; UDI-DI: 278HC0910003M0; Lot Numbers: 1880652, 1880653, 1880654, 1880655, 1880656, 188065… a. Model Number: HC-09100-03M; UDI-DI: 278HC0910003M0; Lot Numbers: 1880652, 1880653, 1880654, 1880655, 1880656, 1880657, 1880658, 1880659, 1880660, 1880661, 1880662, 1880663, 1880664, 1880665, 1880666, 1880667, 1880668, 1880669, 1880670, 1880671, 1880672, 1880673, 1880674, 1880675, 1880676, 1880677, 1880678, 1880679, 1880680, 1880681, 1880682, 1880683, 1880684, 1880685. b. Model Number: HC-10100-03M; UDI-DI: B278HC1010003M0; Lot Numbers: 1880686, 1880687, 1880688, 1880689, 1880690, 1880691, 1880692, 1880693, 1880694, 1880695, 1880696, 1880697, 1880698, 1880699, 1880700, 1880701, 1880702, 1880703, 1880704, 1880705, 1880706, 1880707, 1880708, 1880709, 1880710, 1880711, 1880712, 1880713, 1880714. c. Model Number: HC-11120-03M; UDI-DI: B278HC1112003M0; Lot Numbers: 1880715, 1880716, 1880717, 1880718, 1880719, 1880720, 1880721, 1880722, 1880723, 1880724, 1880725, 1880726, 1880727, 1880728, 1880729, 1880730, 1880731, 1880732, 1880733, 1880734, 1880735, 1880736, 1880737, 1880738, 1880739,

code_info

a. Model Number: HC-09100-03M; UDI-DI: 278HC0910003M0; Lot Numbers: 1880652, 1880653, 1880654, 1880655, 1880656, 188065…

a. Model Number: HC-09100-03M; UDI-DI: 278HC0910003M0; Lot Numbers: 1880652, 1880653, 1880654, 1880655, 1880656, 1880657, 1880658, 1880659, 1880660, 1880661, 1880662, 1880663, 1880664, 1880665, 1880666, 1880667, 1880668, 1880669, 1880670, 1880671, 1880672, 1880673, 1880674, 1880675, 1880676, 1880677, 1880678, 1880679, 1880680, 1880681, 1880682, 1880683, 1880684, 1880685. b. Model Number: HC-10100-03M; UDI-DI: B278HC1010003M0; Lot Numbers: 1880686, 1880687, 1880688, 1880689, 1880690, 1880691, 1880692, 1880693, 1880694, 1880695, 1880696, 1880697, 1880698, 1880699, 1880700, 1880701, 1880702, 1880703, 1880704, 1880705, 1880706, 1880707, 1880708, 1880709, 1880710, 1880711, 1880712, 1880713, 1880714. c. Model Number: HC-11120-03M; UDI-DI: B278HC1112003M0; Lot Numbers: 1880715, 1880716, 1880717, 1880718, 1880719, 1880720, 1880721, 1880722, 1880723, 1880724, 1880725, 1880726, 1880727, 1880728, 1880729, 1880730, 1880731, 1880732, 1880733, 1880734, 1880735, 1880736, 1880737, 1880738, 1880739,

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-1883-2025%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.