CLASS III Device recall · Reported 7 Dec 2016 · FDA Enforcement Report
Dynasty Liners recalled by MicroPort Orthopedics
MicroPort Orthopedics is recalling Dynasty Liners, distributed nationwide in the US. The recall was initiated on 21 Jun 2016 and the FDA has classified it as Class III.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0684-2017
- FDA event ID
- 75063
- Recalling firm
- MicroPort Orthopedics, Arlington, TN
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 21 Jun 2016
- FDA classified
- 1 Dec 2016
- Reported
- 7 Dec 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Foreign Material
- Device type
- Other Medical Devices
Timeline
| 21 Jun 2016 | Recall initiated by company | |
| 1 Dec 2016 | Classified by FDA | +163 days |
| 7 Dec 2016 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Revision rate trends from within the MicroPort Orthopedics Inc. database evaluated for the modular head Metal on Metal THA systems show an increasing overall trend from 2009 to present and it was found that there was a specific hazard/harm for suspected tissue reaction to metal debris over one percent for modular head CONSERVE(R) systems and DYNASTY(R) metal acetabular liner systems.
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
Dynasty Liners: REF DLCOGA28, REF DLCOGB32, REF DLCOGC36, REF DLCOGD38, REF DLCOGE40, REF DLCOGF42, REF DLCOGG44, REF DLCOGH48, REF DLCOGJ52, REF DLCOGK56, For use with the conserve metal head
Where it was distributed
Worldwide Distribution - US (nationwide) Argentina, Australia, Austria, Belgium, Brazil, Bulgaria, Canada, China, Columbia, Cyprus, Czech Republic, Denmark, Finland, France, Georgia, Germany, Greece, Iran, Italy, Jamaica, Japan, Lithuania, Malaysia, Philippines, Poland, Portugal, Russia, Slovenia, South Africa, South Korea, Spain, Switzerland, Taiwan, Netherlands, Turkey, Arab Emirates, United Kingdom, and Vietnam.
Questions about this recall
Why was it recalled?
Revision rate trends from within the MicroPort Orthopedics Inc. database evaluated for the modular head Metal on Metal THA systems show an increasing overall trend from 2009 to present and it was found that there was a specific hazard/harm for suspected tissue reaction to metal debris over one percent for modular head CONSERVE(R) systems and DYNASTY(R) metal acetabular liner systems.
Which lots are affected?
Serial Numbers: REF DLCOGA28 Seral Numbers: 1509498, 1509897, 107461555, 117476083, 127477625, 0411341968, 0611341969, 0901199714 REF DLCOGB32 Serial Numbers: 1428321, 027403682, 027403684, 027412214, 027412216, 027412218, 027412220, 027412222, 029789268, 048571448, 058605178, 068625411, 069837383, 078628910, 079859721, 087467577, 097474918, 097476396, 097477626, 098657540, 099905615, 099927666, 0101018635, 107480309, 107486655, 109968495, 0111248666, 0111254637, 117486656, 117501983, 119982392, 127504540, 127508429, 0211298850, 0211298851, 0401072608, 0501123237, 0601150684, 0711370347, 0711370832, 0711371855, 0711388872, 0801184970, 0801185465, 0901196484, 0901199209, 0901200444, 0901200704 REF DLCOGC36 Serial Numbers: 1389336, 1411596, 1412300, 1419309, 1421706, 1421872, 1421873, 1425040, 1425041, 1426635, 1441425, 1447128, 1448009, 017395680, 017396168, 017398843, 019752394, 027406078, 027406080, 027406549, 027408437, 027408506, 027412667, 029797073,038565179, 038571449, 039808007, 039823319, 039830311, 058576611, 059835277, 059843767, 059859139, 059869515, 067444752, 068608657, 069876613, 069885333, 077449136, 078628911, 078648401, 078648402, 086356142, 086364960, 087462096, 089905617, 089920491, 089924903, 097475888, 097475891, 097475892, 099932177, 099937595, 0101009548, 108705038, 109966090, 0111273375, 0111274786, 118728271, 119975127, 127506074, 127508430, 127514978, 129979634, 129990530, 0201044377, 0201044378, 0201048252, 0201071222, 0211301143, 0301068674, 0301084452, 0401085769, 0501125124, 0611343376, 0611343377, 0611365354, 0611366004, 0611366646, 0701164679, 0701165562, 0701178783, 0801190509, 0901189893, 0901191386, 0901200880, 0901201441, 0901201663 REF DLCOGD38 Serial Numbers: 1390011, 1422255, 1422256, 017395681, 017396169, 019751147, 019752153, 027404999, 027405000, 027408507, 027408521, 027411898, 027412100, 029793006, 038565180, 038571452, 039808008, 039823320, 039831045, 048576612, 049839752, 059846062, 059846677, 059868799, 059869517, 067445955, 067447299, 068608658, 069884531, 069888788, 077459273, 078628912, 078648403, 087464200, 087466701, 089901144, 089911489, 089922646, 096362335, 096374885, 097472362, 097474113, 097476397, 099932178, 099933792, 099937596, 0101038419, 0101038420, 107482012, 107486663, 108706223, 108716643, 108720178, 109941938, 109970863, 0111274868, 0111274869, 117486664, 117489826, 117501984, 118731716, 119980968, 127466702, 127504541, 127508431, 127512298, 128748672, 129990531, 0201062908, 0301062907, 0301067280, 0301067281, 0301081677, 0401096840, 0401098166, 0401109395, 0501127076, 0511344345, 0601147758, 0601148281, 0601148932, 0611344346, 0611346090, 0611346455, 0701172549, 0801192624, 0801193584, 0801193987, 0801194817, 0901192045, 0901203167, 0901206932, 1001206425, 1291016257, 1291016258, 1291019953, 1291019954, 08991148910 REF DLCOGE40 Serial Numbers: 1383898, 1422893, 017395849, 017396101, 017397513, 017398320, 019747416, 019749028, 019752393, 027404377, 027404964, 027406550, 027406551, 027407780, 039802355, 039809788, 039826200, 048571453, 048571454, 049834730, 049839160, 067436735, 069859138, 069868803, 069869518, 076357782, 077440680, 077453681, 078595478, 078595479, 078648404, 078648405, 079888789, 086362336, 087460119, 087460601, 089904051, 089920496, 096372317, 097472371, 097476398, 099931104, 099933793, 0101022064, 0101022065, 0101030547, 0101030548, 0101042594, 0101042595, 107482014, 107486667, 107486668, 107489825, 109941939, 109944905, 0111271873, 0111272250, 117489816, 117501985, 118722756, 118731717, 119980969, 127504542, 127508432, 127512297, 129990532, 0201057245, 0201064292, 0211295490, 0211301165, 0211302281, 0301064291, 0301081699, 0301083868, 0301084453, 0301095292, 0401095291, 0401096841, 0601165833, 0601165834, 0611361690, 0611361691, 0611364735, 0701170121, 0701170775, 0701171294, 0801194833, 0901194835, 0901207002, 0901208793, 0901208953 REF DLCOGF42 Serial Numbers: 1199809, 1366660, 1422894, 1423547, 017396170, 017397514, 017397515, 017398844, 027406424, 027406553, 027411519, 027411895, 027411896, 027413499, 029789333, 029789334, 029798203, 029809789, 029814314, 029819342, 037413500, 039819343, 049833519, 049839753, 058608659, 059846676, 059857910, 068595480, 069883241, 077449093, 078634682, 078634683, 078648406, 079860580, 079887540, 079894027, 086370088, 087462468, 089914628, 096372318, 097472373, 097476399, 099904052, 099931103, 0101022066, 0101030549, 0101030550, 107482016, 107486669, 107486670, 108705039, 108716644, 109922647, 109937597, 109943610, 109966091, 0111276618, 117496631, 117501986, 118728903, 118744506, 119972083, 127504543, 127509428, 127514975, 127514976, 128749026, 128751278, 129990533, 0201053787, 0201053788, 0201062909, 0201062910, 0201068675, 0211299901, 0301071223, 0301081700, 0301083869, 0401104095, 0401104096, 0501127409, 0611346456, 0701167385, 0701168088, 0701168230, 0701169430, 0701170051, 0711367085, 0901208997, 0901209918, 0901209977, 1101247355, 1101248443, 010103054910 REF DLCOGG44 Serial Numbers: 1383128, 1383366, 1392621, 1428789, 017396171, 017397398, 027404375, 027404965, 027406552, 027408531, 027412079, 027412080, 027412086, 029792981, 029793005, 029799054, 029799055, 038565181, 039828320, 039832455, 048571456, 048576613, 049828319, 049830312, 049839159, 057438911,058608660, 059855232, 059857911, 059860406, 059869519, 067445525, 069888790, 077447460, 077459517, 078608662, 078628913, 078648407, 078657546, 079894757, 087464126, 089915880, 089922080, 096362338, 096374886, 097476400, 097476401, 097480312, 098694868, 098706224, 099932179, 099934263, 099939751, 0101025139, 0101025144, 0101027410, 0101038421, 0101038422, 0101046891, 107481184, 107486653, 107487346, 108705037, 108716645, 108723278, 109966092, 117495711, 117495712, 117505591, 118730735, 118744505, 119975128, 119975129, 127504544, 127513338, 127518295, 127522391, 128747417, 128748669, 129998770, 129998777, 0201057246, 0201059716, 0201059717, 0201076758, 0211275710, 0301076757, 0301085876, 0301085877, 0301099035, 0301099036, 0311294091, 0311295489, 0401099037, 0401100077, 0401100078, 0401106374, 0401112729, 0411306527, 0411307069, 0601153393, 0601154045, 0601155591, 0801181073, 0801181695, 0801181920, 0801183924, 0801199319, 0901210490, 1001213377, 1001214138, 1101232813, 1201256582, 1201256583, 1201257832, 1291000319, 1291000321, 1291025140 REF DLCOGH48 Serial Numbers: 027403685, 027403686, 027410682, 027412223, 027412224, 027412225, 027412226, 078608663, 078648408, 078648409, 089904664, 097471988, 097476402, 097476542, 097477627, 0101042593, 107481183, 109967195, 0111277921, 117486671, 117496632, 127504545, 127508400, 127518297, 0201072609, 0401089450, 0601147117, 0901187425, 1101231165, 1291014716 REF DLCOGJ52 Serial Numbers: 099898795, 0101023111, 0201049895, 0201049896 REF DLCOGK56 Serial Numbers: 099898794, 0201023112, 0201049903, 0201052602, 0201052603
Where was it sold?
Worldwide Distribution - US (nationwide) Argentina, Australia, Austria, Belgium, Brazil, Bulgaria, Canada, China, Columbia, Cyprus, Czech Republic, Denmark, Finland, France, Georgia, Germany, Greece, Iran, Italy, Jamaica, Japan, Lithuania, Malaysia, Philippines, Poland, Portugal, Russia, Slovenia, South Africa, South Korea, Spain, Switzerland, Taiwan, Netherlands, Turkey, Arab Emirates, United Kingdom, and Vietnam.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
5 other products · FDA event 75063| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS III | Procotyl (Rim- Lock) Liners recalled by MicroPort Orthopedics | MicroPort Orthopedics | Foreign Material | Nationwide | |
| CLASS III | Conserve Cups recalled by MicroPort Orthopedics | MicroPort Orthopedics | Foreign Material | Nationwide | |
| CLASS III | Conserve Shells recalled by MicroPort Orthopedics | MicroPort Orthopedics | Foreign Material | Nationwide | |
| CLASS III | Lineage Shell recalled by MicroPort Orthopedics | MicroPort Orthopedics | Foreign Material | Nationwide | |
| CLASS III | Lineage Liners recalled by MicroPort Orthopedics | MicroPort Orthopedics | Foreign Material | Nationwide |
More recalls from MicroPort Orthopedics
All 31Other Other Medical Devices recalls
All 13,908| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Plastics Tray kits recalled by Avid Medical | Avid Medical | Foreign Material | Nationwide |
| Device | CLASS II | Heart Prep Tray kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Pack Open Heart Cfh kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Sperm Ab Elisa (96 well plate test) recalled by DRG International | DRG International | Other | Nationwide |
| Device | CLASS III | BeneView Series recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |