Reported Sep 29, 2021 · Terminated
Univation X System knee implant devices as follows
Aesculap Implant Systems LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Aesculap Implant Systems LLC · 3773 Corporate Pkwy · Center Valley, PA · 18034-8217
Is this the product you have?
Univation X System knee implant devices as follows
6 of 6 products
| # | Product as published |
|---|---|
| 1 | Catalog/Product: NL482 UNIVATION F MENISCAL COMP.T1 RM/LM 9MM |
| 2 | NL483 UNIVATION F MENISCAL COMP.T2 RM/LM 9MM |
| 3 | NL484 UNIVATION F MENISCAL COMP.T3 RM/LM 9MM |
| 4 | NL485 UNIVATION F MENISCAL COMP.T4 RM/LM 9MM |
| 5 | NL486 UNIVATION F MENISCAL COMP.T5 RM/LM 9MM |
| 6 | NL487 UNIVATION F MENISCAL COMP.T6 RM/LM 9MM |
- Lot codes and dates
- All lots
This recall covers 8 products
The agency filed one notice per product. You are reading one of them; the other 7 are below.
Where it was sold
- Nationwide
Why it was recalled
Malfunction- loosening of the implant resulting in a potential revision surgery
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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