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UNIVATION XF
Aesculap AG · Model NM622 · UDI-DI 04046963963880
HWT
Prescription
10
510(k) clearances
16,914
Adverse events
85
Recalls
430
Facilities
Description
UNIVATION XF MENISCUS TRIAL SPACER 9MM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-06-27 | LINK BIO CORP | The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The markings on two arms of the instrument were mixed up because the triangular Patella Sizing Template was inse |
| 2022-07-13 | Materialise USA LLC | MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was shipped with the Anatomical Model of case MU22-NOF-SAK |
| 2022-06-29 | DePuy Orthopaedics, Inc. | Manufactured with a Galvanized High Carbon Steel spring instead of the correct 302 Stainless steel spring. has the potential to oxidize and corrode in the ATTUNE Measured Sizing & |
| 2017-12-20 | Integra LifeSciences Corp. | Incidents of stem trial breakage were reported to the firm suggesting that these fractures all occurred during insertion/impaction or extraction of the humeral stem trial whiling p |
| 2017-08-10 | Aesculap Implant Systems LLC | The NS357R Vega PS Tibia Trial/Preparation Plateau size T4 may be incorrectly labeled. If the incorrect size trial is used the potential risk is implantation of the incorrect impl |
| 2017-04-11 | Biomet Microfixation, LLC | Part of the number on the tray lid differ from the part number on the base. |
| 2015-06-24 | Encore Medical, Lp | The markings on the distal face of the instruments are mis-oriented by 180. This includes Anterior and Posterior, which the surgeon uses to correctly place the cut block on the res |
| 2015-06-03 | Biomet, Inc. | Oxford Femoral Drill Guide Lateral IM Adapter may have an undersized diameter that can cause an interference with PN: 32-422822, Oxford Microplasty IM Link. |
| 2014-09-24 | Biomet, Inc. | An investigation identified that the product was incorrectly manufactured as a left humeral trial but is etched as a right humeral trial. |
| 2014-03-28 | DePuy Orthopaedics, Inc. | Urgent Device Correction notifications are being sent to USA distributors with follow-up to surgeons concerning updated surgical techniques stressing the possibility of the shoulde |
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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.