FDA Device Recalls

Recalls /

#204599

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

FDA product code
JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Device class
Class 2
Medical specialty
Orthopedic
510(k) numbers
K223252
Affected lot / code info
a) 02-023-02-0029, GTIN 10885862596376, Serial Numbers: A704613, A704614, A704618, A704633, A704634, A704649, A704651, A704632; b) 02-023-02-0032, GTIN 10885862596383, Serial Numbers: A703837, A703844, A703847, A703863, A704084, A704089, A704100, A704102, A704105, A704110, A704111, A704115, A704142, A704161, A704162, A704167, A704171, A704189, A704190, A704151, A704156, A704183; c) 02-023-02-0035, GTIN 10885862596390, Serial Numbers: A704258, A704282, A704299, A704300, A704306, A704314, A704320; d) 02-023-02-0038, GTIN 10885862596406, Serial Numbers: A704222, A704229, A704231, A704233, 704240, A704249; e) 02-024-35-1512, GTIN 10885862596741, Serial Numbers: A713224, A713230, A713233, A713234, A713237; f) 02-024-35-1515, GTIN 10885862596772, Serial Numbers: A697051; g) 02-024-35-1519, GTIN 10885862596796, Serial Numbers: A713345; h) 02-024-35-2010, GTIN 10885862596819, Serial Numbers: A701145, A701149, A701150, A701151, A701152, A701153, A701154, A701155, A701156, A701157, A701158, A701159, A701160, A701162, A701163, A701164, A701165, A701166; i) 02-024-35-2013, GTIN 10885862596840, Serial Numbers: A697420, A697421, A697423, A697424, A697425, A697427, A697428, A697430, A697431, A697434, A697435, A697437, A697438, A697439, A697440; j) 02-024-35-2015, GTIN 10885862596864, Serial Numbers: A701404, A701405, A701407, A701409, A701410, A701411, A701412, A701417, A701421, A701425, A701426, A701427, A701429, A701434; k) 02-024-35-2509, GTIN 10885862596895, Serial Numbers: A702432, A702433, A702436, A702437, A702438, A702439, A702440, A702441, A702442, A702443, A702444, A702447, A702448, A702449, A702450, A702452, A702453, A702454; l) 02-024-35-2510, GTIN 10885862596901, Serial Numbers: A713194, A713195, A713199, A713203, A713205; m) 02-024-35-2511, GTIN 10885862596918, Serial Numbers: A700853, A700855, A700857, A700859, A700863, A700865, A700866, A700869, A700873, A700874, A700876, A700877, A700880, A700882, A700883, A700887, A700891; n) 02-024-35-2512, GTIN 10885862596925, Serial Numbers: A713238, A713241, A713242, A713243, A713244, A713245, A713246, A713247, A713249, A713250, A713252, A713253, A713254, A713255, A713256, A713257, A713258, A713239; o) 02-024-35-3010, GTIN 10885862596994, Serial Numbers: A701111, A701116, A701117, A701119, A701120, A701121, A701122, A701125, A701126, A701127, A701128, A701130, A701131, A701133, A701137, A701138, A701140, A701141; p) 02-024-35-3011, GTIN 10885862597007, Serial Numbers: A707591, A707592, A707593, A707595, A707597, A707598, A707600, A707601; q) 02-024-35-3012, GTIN 10885862597014, Serial Numbers: A701456, A701458, A701459, A701460, A701463, A701464, A701465, A701466, A701467, A701468, A701469, A701470, A701471, A701472, A701473, A701474, A701476, A701478; r) 02-024-35-3013, GTIN 10885862597021, Serial Numbers: A696988; s) 02-024-35-3513, GTIN 10885862597113, Serial Numbers: A702455, A702458, A702459, A702460, A702462, A702464, A702465, A702466, A702467, A702469, A702470, A702471, A702472, A702473, A702474, A702475, A702476, A702477; t) 02-024-35-3515, GTIN 10885862597137, Serial Numbers: A707603, A707606, A707607; u) 02-024-35-4012, GTIN 10885862597199, Serial Numbers: A702364, A702365, A702366, A702369, A702370, A702371, A702372, A702373, A702375, A702376, A702377, A702378, A702379, A702380, A702381, A702382, A702384, A702385; v) 02-024-35-4013, GTIN 10885862597205, Serial Numbers: A702387, A702389, A702391, A702392, A702393, A702394, A702395, A702396, A702397, A702400, A702401, A702402, A702403, A702404, A702405, A702406, A702407, A702408; w) 02-024-35-4510, GTIN 10885862597267, Serial Numbers: A702341, A702342, A702343, A702345, A702346, A702347, A702349, A702350, A702351, A702352, A702353, A702354, A702355, A702357, A702358, A702359, A702360, A702361; x) 02-024-35-4515, GTIN 10885862597311, Serial Numbers: A707570, A707572, A707573, A707574, A707575, A707576, A707578, A707579, A707580, A707581, A707582, A707583, A707584, A707585, A707586.A707587, A707589, A707590; y) 02-024-35-5011, GTIN 10885862597366, Serial Numbers: A706709, A706710, A706711, A706712, A706714, A706715, A706716, A706717, A706719, A706720, A706721, A706722, A706723, A706724, A706726, A706727, A706729, A706730; z) 02-024-35-5012, GTIN 10885862597373, Serial Numbers: A706791, A706792, A706793, A706794, A706795, A706796, A706797, A706798, A706800, A706801, A706802, A706803, A706804, A706805, A706806, A706807, A706808, A706809; aa) 02-024-44-1511, GTIN 10885862597724, Serial Numbers: A750655, A750656, A750657, A750659, A750660, A750665, A750667, A750669; bb) 02-024-44-2009, GTIN 10885862597793, Serial Numbers: A769691, A769693, A769694, A769695, A769700, A769701, A769702, A769707; cc) 02-024-44-2011, GTIN 10885862597816, Serial Numbers: A750725, A750726, A750729, A750737, A750738, A750739, A750745, A750750; dd) 02-024-44-2015, GTIN 10885862597854, Serial Numbers: A750751, A750753, A750756, A750757, A750761, A750762, A750764, A750768; ee) 02-024-44-2510, GTIN 10885862597892, Serial Numbers: A753626, A753627, A753632, A753633, A753637, A753639, A753645, A753648; ff) 02-024-44-2515, GTIN 10885862597946, Serial Numbers: A753165, A753166, A753171, A753172, A753174, A753176, A753177, A753185; gg) 02-024-44-3009, GTIN 10885862597977, Serial Numbers: A769185, A769195, A769198, A769200, A769202, A769204, A769208, A769217; hh) 02-024-44-3011, GTIN 10885862597991, Serial Numbers: A753080, A753085, A753086, A753092, A753093, A753096, A753099, A753103; ii) 02-024-44-3013, GTIN 10885862598011, Serial Numbers: A753187, A753188, A753189, A753193, A753196, A753198, A753204, A753209; jj) 02-024-44-3015, GTIN 10885862598035, Serial Numbers: A753057, A753063, A753065, A753070, A753071, A753072, A753073, A753074; kk) 02-024-44-3509, GTIN 10885862598066, Serial Numbers: A769635, A769649, A769652, A769655, A769656, A769657, A769658, A769661; ll) 02-024-44-4009, GTIN 10885862598158, Serial Numbers: A769669, A769672, A769675, A769676, A769680, A769683, A769685, A769689; mm) 02-024-44-4509, GTIN 10885862598240, Serial Numbers: A769149, A769150, A769151, A769152, A769154, A769159, A769162, A769173; nn) 02-024-44-4511, GTIN 10885862598264, Serial Numbers: A761277, A761292, A761293, A761294, A761295, A761296, A761297, A761298; oo) 02-024-44-4512, GTIN 10885862598271, Serial Numbers: A761302, A761304, A761305, A761306, A761309, A761310, A761311, A761312; pp) 02-024-44-4513, GTIN 10885862598288, Serial Numbers: A760921, A760924, A760929, A760930, A760931, A760932, A760934, A760938; qq) 02-024-44-5013, GTIN 10885862598370, Serial Numbers: A761213, A761214, A761215, A761218, A761220, A761221, A761228, A761229

Why it was recalled

Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.

Root cause (FDA determination)

Packaging change control

Action the firm took

Exactech issued an URGENT MEDICAL DEVICE RECALL notice to its direct consignees on 11/21/2023 via email. The notice explained the issue, clinical impact, and requested the removal and return of all affected products. 11/22/2023, the firm initiated the recall OUS also by email.

Recalling firm

Firm
Exactech, Inc.
Address
2320 Nw 66th Ct, Gainesville, Florida 32653-1630

Distribution

Distribution pattern
US NY, TX, IN, IL, MN, KY, VA, MD, TN, GA, NH, ME, SC, NV, FL, AR and Australia, Brazil, Chile, France, Germany, Guatemala, Italy, Japan, Korea, Slovenia, Spain, UK

Timeline

Recall initiated
2023-11-21
Posted by FDA
2024-01-18
Status

Source: openFDA Device Recall endpoint. Recall record ID #204599. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.