Exactech Truliant — Class II medical device recall Z-0586-2024
Ongoing recall by Exactech, Inc., reported 2023-12-27, distributed in AR, FL, GA, IL, IN, KY, MD, ME…. Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.
| Recall number | Z-0586-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Exactech, Inc., Gainesville, FL, United States |
| Recall initiated | 2023-11-21 |
| Classified | 2023-12-19 |
| Reported by FDA | 2023-12-27 |
| Distributed | AR, FL, GA, IL, IN, KY, MD, ME, MN, NH, NV, NY, SC, TN, TX, VA |
| Countries outside the US | AU, BR, CL, DE, ES, FR, GB, GT, IT, JP, KR, SI |
| UPC / GTIN / UDI-DI | 10885862596376, 10885862596383, 10885862596390, 10885862596406, 10885862596741, 10885862596772, 10885862596796, 10885862596819, 10885862596840, 10885862596864, 10885862596895, 10885862596901, 10885862596918, 10885862596925, 10885862596994, 10885862597007, 10885862597014, 10885862597021, 10885862597113, 10885862597137, 10885862597199, 10885862597205, 10885862597267, 10885862597311, 10885862597366 and 18 more |
| Serial numbers | 704240, A696988, A697051, A697420, A697421, A697423, A697424, A697425, A697427, A697428, A697430, A697431, A697434, A697435, A697437, A697438, A697439, A697440, A700853, A700855, A700857, A700859, A700863, A700865, A700866 and 440 more |
Product
Exactech Truliant, Activit-E Knee Insert, Catalog Numbers: a) 02-023-02-0029, b) 02-023-02-0032, c) 02-023-02-0035, d) 02-023-02-0038, e) 02-024-35-1512, f) 02-024-35-1515, g) 02-024-35-1519, h) 02-024-35-2010, i) 02-024-35-2013, j) 02-024-35-2015, k) 02-024-35-2509, l) 02-024-35-2510, m) 02-024-35-2511, n) 02-024-35-2512, o) 02-024-35-3010, p) 02-024-35-3011, q) 02-024-35-3012, r) 02-024-35-3013, s) 02-024-35-3513, t) 02-024-35-3515, u) 02-024-35-4012, v) 02-024-35-4013, w) 02-024-35-4510, x) 02-024-35-4515, y) 02-024-35-5011, z) 02-024-35-5012, aa) 02-024-44-1511, bb) 02-024-44-2009, cc) 02-024-44-2011, dd) 02-024-44-2015, ee) 02-024-44-2510, ff) 02-024-44-2515, gg) 02-024-44-3009, hh) 02-024-44-3011, ii) 02-024-44-3013, jj) 02-024-44-3015, kk) 02-024-44-3509, ll) 02-024-44-4009, mm) 02-024-44-4509, nn) 02-024-44-4511, oo) 02-024-44-4512, pp) 02-024-44-4513, qq) 02-024-44-5013
Reason for recall
Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0586-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.