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 month

Severity split

Class I 0 0%Class II 50 100%Class III 0 0%

Why linkbio is recalled

By year

Ongoing linkbio recalls

50 active

All linkbio recalls, newest first

50 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IICore Workstation, a component of the Core Shoulder System recalledLinkbioOtherNationwide
DeviceCLASS IILINK SymphoKnee System L-Shaped Femoral Augment recalled by LinkbioLinkbioPackaging DefectsNationwide
DeviceCLASS IILink Sled Knee System: All Poly Tibial Component recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System: All Poly Tibial Component recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System: All Poly Tibial Component recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System: Endo Sled Knee Fem Comp, Medium recalledLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System Porex Endo Sled Knee Fem Comp, Large recalledLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System: All Poly Tibial Component 9X58MM recalledLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System Porex Endo recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System: Endo recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System: All Poly Tibial Component recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System Porex Endo recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System: All Poly Tibial Component recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System: Endo recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System Porex Endo recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System Porex Endo recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System Endo recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System Endo recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System Porex Endo recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System Endo recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System Endo recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System Endo recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System Endo recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System: All Poly Tibial Component recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System: Endo Sled Knee Fem Comp, Small recalledLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System: All Poly Tibial Component 11X58MM recalledLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System Porex Endo recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System: All Poly Tibial Component recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System Endo recalled by LinkbioLinkbioSterilityNV, NY
DeviceCLASS IILink Sled Knee System Endo recalled by LinkbioLinkbioSterilityNV, NY

About 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.