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AESCULAP

Aesculap AG · Model NK060K · UDI-DI 04046963110628

KWY Prescription
10
510(k) clearances
16,502
Adverse events (49 deaths)
88
Recalls
214
Facilities

Description

BIPOLAR CUP ID28MM OD60MM SELF-CENTERING

Recalls

DateFirmReason
2025-09-23Total Joint Orthopedics, Inc.Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is impla
2025-09-09BioPro, Inc.Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is impla
2024-10-15Smith & Nephew, Inc.The Bipolar assembly contains an oversized Retainer Ring.
2024-04-26Exactech, Inc.The AcuMatch L-Series 22mm Inner Diameter Bipolar Hip Liner lots were packaged without the specified ethylene vinyl alcohol (EVOH) layer. Between 2004 and August 2021, our packagin
2020-02-26Biomet, Inc.Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
2020-02-26Biomet, Inc.Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
2020-02-26Biomet, Inc.Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
2020-02-26Biomet, Inc.Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
2020-02-26Biomet, Inc.Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
2020-02-26Biomet, Inc.Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.