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Libertas
MAXX ORTHOPEDICS, INC. · Model MO-MLLH-MK/40 · UDI-DI 00810008124635
1
510(k) clearances
172
Adverse events
4
Recalls
94
Facilities
Description
Modular E-XLPE Liner Size MK/40 Elevated Wall
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-31 | Exactech, Inc. | Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer. |
| 2024-12-31 | Exactech, Inc. | Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer. |
| 2023-11-21 | Exactech, Inc. | Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag. |
| 2022-08-25 | Zimmer, Inc. | The outer sterile package cavity has a corner wall thickness that is below the specification. The thin corner wall could potentially crack during transit. Potential risks include n |
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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.