Z-1880-2025Class II

Segmental Stem, Cemented, Bowed, 152MM, 1 EACH. Model Numbers: CB-11152-03M, CB-13152-03M, CB-15152-03M...

Name: Z-1880-2025 Segmental Stem, Cemented, Bowed, 152MM, 1 EACH. Model Numbers: CB-11152-03M, CB-13152-03M, CB-15152-03M...
Creator: Onkos Surgical, Inc.
Published: 2023-09-01
License: https://open.fda.gov/license/

Onkos Surgical, Inc. / initiated 2023-09-01 / Open, Classified / root cause: packaging

FDA source

Onkos Surgical, Inc. began a recall of 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 on 2023-09-01. FDA classified it as Class II and gives the reason as "Potential for breach of Tyvek seals". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as packaging.

Recall record

Recall number: Z-1880-2025
Classification: Class II
Status: Open, Classified
Initiated: 2023-09-01
Posted: 2025-05-29
Recalling firm: Onkos Surgical, Inc.
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
Product code: KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
Reason for recall: Potential for breach of Tyvek seals.
Root cause tag: packaging
FDA root cause: Packaging change control
Action: Onkos Surgical began notifying consignees on about 09/01/2023 via email. Consignees were instructed to complete and return the response form providing the affected lot numbers being returned, coordinate the return of affected units, and to note that when placing these parts into totes, always place them flat.
Quantity in commerce: 49 units
Distribution: Product was shipped from Onkos' distribution in Olive Branch, MS to consignees in the following states: GA, TX, WA, LA, NJ, FL, AZ, MD, MS, KS, IL, WI, KY, PA, NC, NE, OH, HI.
Product codes and lots: a. Model Number: CB-11152-03M; UDI-DI: B278CB1115203M0; Lot Numbers: 1880259, 1880260, 1880261, 1880262, 1880263, 1880264, 1880265, 1880266, 1880267, 1880268, 1880269, 1880270, 1880271, 1880272, 1880273, 1880274. b. Model Number: CB-13152-03M; UDI-DI: B278CB1315203M0; Lot Numbers: 1880275, 1880276, 1880277, 1880278, 1880279, 1880280, 1880281, 1880282, 1880283, 1880284. c. Model Number: CB-15152-03M; UDI-DI: B278CB1515203M0; Lot Numbers: 1880285, 1880286, 1880287, 1880288, 1880289, 1880290, 1880291, 1880292, 1880293, 1880294, 1880295, 1880296. d. Model Number: CB-17152-03M; UDI-DI: B278CB1715203M0; Lot Numbers: 1880297, 1880298, 1880299, 1880300, 1880301, 1880302, 1880303, 1880304, 1880305, 1880306, 1880307.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1880-2025
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1879-2025	Class II	Ongoing	Voluntary: Firm initiated	2025-06-04	2025-05-29
Z-1880-2025	Class II	Ongoing	Voluntary: Firm initiated	2025-06-04	2025-05-29
Z-1881-2025	Class II	Ongoing	Voluntary: Firm initiated	2025-06-04	2025-05-29
Z-1882-2025	Class II	Ongoing	Voluntary: Firm initiated	2025-06-04	2025-05-29
Z-1883-2025	Class II	Ongoing	Voluntary: Firm initiated	2025-06-04	2025-05-29
Z-1884-2025	Class II	Ongoing	Voluntary: Firm initiated	2025-06-04	2025-05-29

Product code KRO

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)