FDA Device recall Z-1879-2025
a. Segmental Stem, Cemented, Straight, 100MM, 1 EACH
- FDA Device
- Class II
- ongoing
- Published 2025-06-04
On 2025-06-04 the FDA classified a Class II recall of a. Segmental Stem, Cemented, Straight, 100MM, 1 EACH by Onkos Surgical, citing potential for breach of Tyvek seals.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1879-2025 |
| 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
a. Segmental Stem, Cemented, Straight, 100MM, 1 EACH; Model Numbers: CS-09100-03M, CS-10100-03M. b. Segmental Stem, Cemented, Straight, 120MM, 1 EACH. Model Numbers: CS-11120-03M, CS-13120-03M, CS-15120-03M, CS-17120-03M. Component. of ELEOS LIMB SALVAGE SYSTEM
Reason
Potential for breach of Tyvek seals.
Identifiers
| code_info | a. Model Number: CS-09100-03M; UDI-DI: B278CS0910003M0; Lot Numbers: 1880308, 1880309, 1880310, 1880311, 1880312, 18803…a. Model Number: CS-09100-03M; UDI-DI: B278CS0910003M0; Lot Numbers: 1880308, 1880309, 1880310, 1880311, 1880312, 1880313, 1880314, 1880315, 1880316, 1880317, 1880318, 1880319, 1880320, 1880321, 1880322, 1880323, 1880324, 1880325, 1880326, 1880327, 1880328, 1880329, 1880330, 1880331, 1880332, 1880333. Model Number: CS-10100-03M. UDI-DI: B278CS1010003M0. Lot Numbers: 1880334, 1880335, 1880336, 1880337, 1880338, 1880339, 1880340, 1880341, 1880342, 1880343, 1880344, 1880345. b. Model Number: CS-11120-03M; UDI-DI: B278CS1112003M0; Lot Numbers: 1880346, 1880347, 1880348, 1880349, 1880350, 1880351, 1880352, 1880353, 1880354, 1880355, 1880356, 1880357, 1880358, 1880359, 1880360, 1880361, 1880362, 1880363, 1880364, 1880365, 1880366, 1880367, 1880368, 1880369, 1880370, 1880371, 1880372, 1880373, 1880374, 1880375, 1880376. Model Number: CS-13120-03M; UDI-DI: B278CS1312003M0; Lot Numbers: 1880377, 1880378, 1880379, 1880380, 1880381, 1880382, 1880383, 1880384, 1880385, 1880386, 1880387, 1880388, |
|---|
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-1879-2025%22
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