Howmedica Osteonics recalls Triathlon Prim CEM FXD BPLT 7 baseplates with potentially oversized internal profiles that may prevent proper locking of the insert. Affected units include Catalog No. 5520B700, Lot JHS2H.
The internal profile of the Triathlon Prim (Baseplate) is potentially oversized; there may be a witness mark (taper) at the bottom of the internal profile of the baseplate, which prevents the insert from locking on the baseplate.
Howmedica Osteonics is recalling Triathlon Prim CEM FXD BPLT 7 baseplates that may have an oversized internal profile. This could prevent the insert from locking securely, potentially causing instability during use.
The baseplate's internal profile may be oversized, creating a witness mark (taper) at the bottom. This prevents the insert from locking properly, which could lead to instability in joint replacements.
Orthopedic surgeons and patients using this specific baseplate model for joint replacements are most at risk. The recall affects units sold with Catalog No. 5520B700 and Lot JHS2H.
Check for the Triathlon Prim CEM FXD BPLT 7 baseplate with Catalog Number 5520B700 and Lot JHS2H. This model is used in orthopedic joint replacements.
Identify if your baseplate has Catalog Number 5520B700 and Lot JHS2H.
The recall indicates a potential issue with the baseplate's internal profile that may prevent proper locking of the insert, but the remedy is not specified in the record.
Check for Catalog Number 5520B700 and Lot JHS2H on the baseplate.
The recall record does not specify a remedy, so no action is required beyond checking product details.
We’ve drafted a message you can send Howmedica Osteonics to request your refund or repair — edit it as you like.
Subject: Recall Z-2329-2021 — Howmedica Osteonics Howmedica Osteonics Hello, I own a Howmedica Osteonics that is covered by recall Z-2329-2021 from Howmedica Osteonics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
