Linkbio Corp.
Linkbio Corp. has 3 FDA enforcement events on this register (50 product records) between 2023 and 2026: 3 device; the busiest year was 2023 with 2.
0% of its events are Class I; the most common class is Class II (3). 3 events are listed as ongoing; the recalling firm's address is in NJ.
Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.
Enforcement events
| Initiated | Product (first record) | Type | Class | Records | Status |
|---|---|---|---|---|---|
| 12 Mar 2026 | LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136. | Device | Class II | 1 | Ongoing |
| 25 Apr 2023 | LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6 Tilastan, cemented. Intended for primary and revision total knee replacement. Item Number: 880-325/13 | Device | Class II | 1 | Ongoing |
| 21 Mar 2023 | LINK SLED Knee System: ENDO SLED KNEE FEM COMP, SMALL Item Number: 15-2020/40 | Device | Class II | 48 | Ongoing |
By type and class
Class I: 0% of this firm's events; 18% of all events on the register.
Events by year
Questions and answers
How many FDA recalls has Linkbio Corp. had?
3 enforcement events (50 product records) on this register, 2023–2026: 3 device.
Are any Linkbio Corp. recalls ongoing?
3 events are listed as ongoing in the current openFDA export.
What class are Linkbio Corp. recalls?
3 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.
Where does this data come from?
openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.
Provenance
Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.