LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136. — FDA record Z-1810-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Mar 12, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.
Reason
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
Classification
Class II
Recalling firm
Linkbio Corp.
Quantity
5 units
Agency-reported status
Ongoing
Source record identifier
Z-1810-2026

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityProduct Code: 87-9136. UDI-DI: 00810022403099. All serial numbers of the CORE Workstation are affected.

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

US Nationwide distribution in the state of Alabama, Florida, and Kansas.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Apr 22, 2026
Recall initiation date
Mar 12, 2026
Center classification date
Apr 10, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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