Linkbio recalls
Linkbio has 50 recalls on record with the FDA and USDA, the earliest in 2023 and the latest reported on 22 Apr 2026. 50 are still ongoing. 1 was reported in the last 12 months. The most frequent reason is sterility.
Total recalls50since 2023
Last 12 months1reported
Class I00% of total
Ongoing50latest 22 Apr 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 50 100%Class III 0 0%
Why linkbio is recalled
Product types
By year
Ongoing linkbio recalls
50 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Core Workstation, a component of the Core Shoulder System recalled | Linkbio | Other | Nationwide |
| Device | CLASS II | LINK SymphoKnee System L-Shaped Femoral Augment recalled by Linkbio | Linkbio | Packaging Defects | Nationwide |
| Device | CLASS II | Link Sled Knee System: All Poly Tibial Component recalled by Linkbio | Linkbio | Sterility | NV, NY |
| Device | CLASS II | Link Sled Knee System: All Poly Tibial Component recalled by Linkbio | Linkbio | Sterility | NV, NY |
| Device | CLASS II | Link Sled Knee System: All Poly Tibial Component recalled by Linkbio | Linkbio | Sterility | NV, NY |
| Device | CLASS II | Link Sled Knee System: Endo Sled Knee Fem Comp, Medium recalled | Linkbio | Sterility | NV, NY |
All linkbio recalls, newest first
50 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.