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Prosthesis, Hip, Femoral Component, Cemented, Metal

FDA product code JDG · Class 2 · Orthopedic

2,917
Registered devices
6,699
Adverse events
18
Recalls
59
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-07-15Waldemar Link GmbH & Co. KG (Mfg Site)Inconsistent size terminology and color coding used on labeling
2025-07-15Waldemar Link GmbH & Co. KG (Mfg Site)Inconsistent size terminology and color coding used on labeling
2024-02-06Waldemar Link GmbH & Co. KG (Mfg Site)Due to two complaints, has come to our attention that additional guidance is required on the correct interpretation of the carton label Size and Type columns to
2024-02-06Waldemar Link GmbH & Co. KG (Mfg Site)Due to two complaints, has come to our attention that additional guidance is required on the correct interpretation of the carton label Size and Type columns to
2024-02-06Waldemar Link GmbH & Co. KG (Mfg Site)Due to two complaints, has come to our attention that additional guidance is required on the correct interpretation of the carton label Size and Type columns to
2024-02-06Waldemar Link GmbH & Co. KG (Mfg Site)Due to two complaints, has come to our attention that additional guidance is required on the correct interpretation of the carton label Size and Type columns to
2021-12-30Howmedica Osteonics Corp.There is a potential label mix between certain lots of Exeter V40 Cemented Hip (125mm) Stem and Exeter V40 Cemented Hip (150mm) Stem.
2021-12-30Howmedica Osteonics Corp.There is a potential label mix between certain lots of Exeter V40 Cemented Hip (125mm) Stem and Exeter V40 Cemented Hip (150mm) Stem.
2021-10-15Howmedica Osteonics Corp.XXX
2021-10-15Howmedica Osteonics Corp.There is a potential for the outer white Tyvek lid to debond from the sealed package.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.