LinkBio CORE Workstation Recall Over Display Error
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Linkbio Corp. is recalling 5 units of the LinkBio CORE Workstation due to a potential display error showing incorrect planning dates, affecting nationwide distribution in Alabama, Florida, and Kansas.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on May 4, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
LinkBio CORE Workstation Recall
What Happened
Linkbio Corp. is recalling the LinkBio CORE Workstation because it may display an incorrect "Planning Date" when viewing cases on the "Start Case" menu screen. This is a voluntary recall initiated by the firm.
Which Products Are Affected
The affected product is the LinkBio CORE Workstation, a component of the CORE Shoulder System, with Product Code: 87-9136. The recall involves 5 units, all serial numbers, and the UDI-DI: 00810022403099. Distribution occurred nationwide in the United States, specifically in the states of Alabama, Florida, and Kansas. The recall number is Z-1810-2026.
What You Should Do
Consumers who have the affected product should contact Linkbio Corp. for instructions, as this is a firm-initiated recall notified via e-mail.
Why This Matters
This recall involves a medical device that could lead to errors in date displays, potentially affecting case planning in a healthcare setting. As a Class II recall, it indicates a situation where adverse health consequences are remote or reversible.
Source
Information is from the FDA recall notice, available at the FDA website under recall number Z-1810-2026.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,199 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to May 4, 2026.
Frequently Asked Questions
Common questions about this FDA recall.