FDA recall record

LinkBio CORE Workstation, a component of the CORE Shoulder System recall — FDA Z-1810-2026

The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.

Class IIclassification
Z-1810-2026official record ID
Apr 22, 2026report date

Recall record at a glance

Official recordZ-1810-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmLinkbio Corp.
Report dateApr 22, 2026
Recall initiation dateMar 12, 2026
Quantity5 units
LocationRockaway, NJ, United States

Official product description

LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.

Why the product was recalled

The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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