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Recall Observatory FDA recall evidence

Device product

Univation X System knee implant devices as follows: Catalog/Product: NL482 UNIVATION F MENISCAL COMP.T1 RM/LM 9MM; NL483 UNIVATION F MENISCAL COMP.T2 RM/LM 9MM; NL484 UNIVATION F MENISCAL COMP.T3 RM/LM 9MM; NL485 UNIVATION F MENISCAL COMP.T4 RM/LM 9MM; NL486 UNIVATION F MENISCAL COMP.T5 RM/LM 9MM; NL487 UNIVATION F MENISCAL COMP.T6 RM/LM 9MM

Z-2511-2021

March 19, 2021

Class II

Product summary

Firm
Aesculap Implant Systems LLC
Event
Event 88325
Status
Terminated
Classification
Class II
Quantity
Unavailable
Official record key
device-enforcement:Z-2511-2021

Official wording

Reason: Malfunction- loosening of the implant resulting in a potential revision surgery

Code information: All lots

Distribution pattern: US Nationwide distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Malfunction- loosening of the implant resulting in a potential revision surgery