Home › WALDEMAR LINK GmbH & Co. KG › LINK Vario-Cup Prosthesis
LINK Vario-Cup Prosthesis
WALDEMAR LINK GmbH & Co. KG · Model 107-220/56 · UDI-DI 04026575329601
KWY
Prescription
1
510(k) clearances
16,502
Adverse events (49 deaths)
88
Recalls
214
Facilities
Description
Vario-Head Cup,self-centering
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-09-23 | Total 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 |
| 2025-09-09 | BioPro, 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 |
| 2024-10-15 | Smith & Nephew, Inc. | The Bipolar assembly contains an oversized Retainer Ring. |
| 2024-04-26 | Exactech, 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 |
| 2020-02-26 | Biomet, Inc. | Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters. |
| 2020-02-26 | Biomet, Inc. | Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters. |
| 2020-02-26 | Biomet, Inc. | Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters. |
| 2020-02-26 | Biomet, Inc. | Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters. |
| 2020-02-26 | Biomet, Inc. | Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters. |
| 2020-02-26 | Biomet, Inc. | Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters. |
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Get your free API keyRead the docsData 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.