Data Foundry

Medical device recalls 2020

Knee Products: 189420 Vanguard Knee System — Class II medical device recall Z-2152-2020

Terminated recall by Biomet, Inc., reported 2020-06-03, distributed nationwide. Potential presence of elevated endotoxin levels that exceed the specification limit

Recall numberZ-2152-2020
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmBiomet, Inc., Warsaw, IN, United States
Recall initiated2020-04-17
Classified2020-05-28
Reported by FDA2020-06-03
Terminated2021-06-25
DistributedNationwide (US)
Countries outside the USCA, CL, CR, IN, JP, MX, NL, SG, TH, TW
Quantity107 units
Reason classessterility
UPC / GTIN / UDI-DI00880304451308, 00880304451322, 00880304451346, 00880304451360, 00880304451735, 00880304454859
Lot numbers530900

Product

Knee Products: 189420 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 63 MM 189422 Vanguard Knee System, PS Mono Lock Tibial Bearing, 12 MM X 63 MM 189442 Vanguard Knee System, PS Mono Lock Tibial Bearing, 12 MM X 67 MM 189460 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM 189440 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 67 MM 189460 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM 189420 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 63 MM 189460 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM 189426 Vanguard Knee System, PS Mono Lock Tibial Bearing, 16 MM X 63 MM 189440 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 67 MM 189460 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 71 MM

Reason for recall

Potential presence of elevated endotoxin levels that exceed the specification limit

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2152-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.