Z-0683-2017Class III

Lineage Liners: REF 70102846, REF 70202852, REF 70202852, REF 70302858, REF 70303258, REF 70402864, REF...

Name: Z-0683-2017 Lineage Liners: REF 70102846, REF 70202852, REF 70202852, REF 70302858, REF 70303258, REF 70402864, REF...
Creator: MicroPort Orthopedics Inc.
Published: 2016-06-21
License: https://open.fda.gov/license/

Microport Orthopedics Inc. / initiated 2016-06-21 / Terminated / root cause: design

FDA source

MicroPort Orthopedics Inc. began a recall of Lineage Liners: REF 70102846, REF 70202852, REF 70202852, REF 70302858, REF 70303258, REF 70402864, REF 70403264, REF 70403664 For use with the conserve metal... on 2016-06-21. FDA classified it as Class III and gives the reason as "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...". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-0683-2017
Classification: Class III
Status: Terminated
Initiated: 2016-06-21
Posted: 2016-12-01
Terminated: 2017-07-01
Recalling firm: Microport Orthopedics Inc.
Product: Lineage Liners: REF 70102846, REF 70202852, REF 70202852, REF 70302858, REF 70303258, REF 70402864, REF 70403264, REF 70403664 For use with the conserve metal head
Product code: LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
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.
Root cause tag: design
FDA root cause: Device Design
Action: MicroPort sent an Urgent Field Safety Notice dated June 22, 2016, to all affected customers notifying them of the change in the instructions for use on July 7th, 2016 by email. The firm also notified US hospitals where the implantation surgeries occurred within the last twelve (12) months by letter on July 13th, 2016 delivered by FedEx Priority. Customers were asked to complete and return the enclosed form even if they do not have any affected product to return by fax to 1-901-451-6032 or [email protected]. For questions regarding this recall call 901-867-4771.
Quantity in commerce: 5,009 units
Distribution: 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.
Product codes and lots: REF 70102846 Serial numbers: 06217334, 06217335, 06217336, 07218879, 10229555, 12339970, 12342378, 09345262, 11356669, 03459689, 03460757, 05478476, 06487845, 09491060, 11497839, 114131987, 025179937, 035198678, 035199154, 075211008, 085258159, 095267627, 085267672, 125294335, 016302354, 026317823, 026322014, 056332874, 056340972, 066346343, 066347890, 066349011, 076361472, 086364785, 086365941, 086365942, 086366614, 027403696, 027405367, 037417244, 037417245, 037423200, 047423201, 057426382, 057436510, 067442040, 067445874, 067447459, 077449134, 077456252, 077456253, 077458343, 087458991, 097465277, 097465278, 107473197, 097476410, 107481165, 107485823, 107486701, 117486702, 117495033, 127500338, 127500339, 038523902, 028523903, 028533974, 028533976, 038533977, 048571510, 048571511, 078595472, 078595473, 108669048, 108694963, 108694964, 118706230, 029763680, 029780243, 069816370, 069829627, 069835276, 069840533, 069841537, 069842578, 069871618, 099893231, 0301059446, 0301059448, 0301059449, 0301076824, 0301080515, 0301084486, 0301084488, 0301085776, 0301089607, 0301089608, 0401112808, 0601145034, 0601146232, 0801172562, 0801172985, 1101217377, 1381687, 1382260 REF 70202852 Serial Numbers: 06217338, 03442273, 03457113, 094103603, 114115155, 114131988, 067444763, 097458085, 117501995, 018507062, 078595474, 022A147720 REF 70202852 Serial Numbers: 022A147721, 022A147722, 022A147723, 022A147723, 022A147724, 06217340, 04217341, 04217342, 04217343, 04218880, 05218881, 04218882, 08225650, 08227481, 08227482, 10228744, 11228846, 03334611, 05335140, 03339967, 03339968, 08342274, 09345234, 08345235, 10349867, 10349868, 10349869, 03455651, 03457114, 03460758, 05478475, 06487846, 08491061, 08497840, 08499658, 094103604, 114115156, 114131989, 015140898, 015145854, 015167730, 025182498, 025182499, 025185569, 035198684, 055208762, 055228595, 055229916, 065242431, 075242432, 065245652, 085258160, 095267361, 095267673, 085267674, 105281165, 115291529, 125292876, 115292878, 016311871, 016311871, 016311872, 026316752, 026317146, 026317824, 026319568, 046326036, 046329102, 056331319, 056342436, 056344951, 066346344, 066349010, 076361473, 086364783, 086365943, 106369766, 116371021, 116373886, 116382786, 037399873, 027403168, 027403697, 027405368, 027408532, 027408593, 027408594, 027409933, 037417800, 037420888, 047423580, 057431859, 057436511, 067444764, 067445875, 067447445, 067447455, 077449135, 077452390, 077453351, 077457329, 097458992, 087459274, 087464167, 087464168, 097464169, 087466761, 087466762, 087466763, 097471664, 107476411, 107481166, 107481167, 107481168, 107488772, 107488773, 117488774, 117500335, 117500336, 127500337, 018507065, 028507066, 028533978, 028533979, 038533980, 038533981, 068571512, 068571513, 068595475, 068595477, 068628972, 078657275, 078657276, 088657277, 088657277, 088666909, 088668637, 088681722, 098688681, 098688682, 108694972, 108694973, 108694974, 108706231, 019744517, 029744518, 029752395, 029752396, 019780244, 069805762, 059805763, 049826202, 039826203, 059832457, 069837384, 059840534, 069841535, 069841536, 069843282, 079843284, 079871619, 099893232, 099894028, 109943611, 109949751, 119976454, 129984899, 0101009599, 0101019757, 0101048257, 0201049093, 0301049096, 0301064289, 0301064290, 0301076825, 0401079670, 0401079671, 0401089609, 0401089610, 0401108733, 0401109165, 0501137724, 0601138315, 0601138736, 0601142035, 0801177943, 0801178058, 0701179671, 0801189482, 0801189732, 1101214882, 1001214883, 1101215441, 0511308183, 0511308908, 0511311535, 1379458, 1379459, 1379605, 1381323, 1384695 REF 70302858 Serial Numbers: 04217339, 10228742, 09491063, 056340187, 106369767, 106373887 REF 70303258 Serial Numbers: 022A147725, 022A147726, 022A147727, 022A147739, 04217344, 04217345, 04217346, 08225648, 08225648, 08227483, 10228741, 10230588, 05335139, 11339972, 03449870, 03460759, 05478477, 06487847, 08491062, 08497841, 114131990, 114131991, 015155783, LLALMD033E, 075208766, 085258161, 125294334, 016308023, 056333740, 066347206, 086364784, 116366898, 116382787, 037417544, 047420889, 057431860, 057436512, 067445876, 067447458, 077451556, 097458361, 097475906, 107481169, 117481170, 107489026, 127500332, 117500333, 127500334, 018507067, 028533983, 098625460, 108716003, 029753067, 079828958, 069843288, 0201044697, 0401085943, 0401092474, 0401092475, 0401106375, 0401107035, 0501132274, 0601143641, 0601151739, 0701165736, 0901197191, 1388534 REF 70402864 Serial numbers: 11228743, 056339647, 066347891 REF 70403264 Serial numbers: 08228131, 056330591 REF 70403664 Serial Numbers: 062A147184, 062A147738, 06217348, 09339971, 11355652, 03457115, 03460761, 05478478, 015140899, 055199111, 075241210, 016303424

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0683-2017
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0683-2017	Class III	Terminated	Voluntary: Firm initiated	2016-12-07	2016-12-01
Z-0684-2017	Class III	Terminated	Voluntary: Firm initiated	2016-12-07	2016-12-01
Z-0685-2017	Class III	Terminated	Voluntary: Firm initiated	2016-12-07	2016-12-01
Z-0686-2017	Class III	Terminated	Voluntary: Firm initiated	2016-12-07	2016-12-01
Z-0687-2017	Class III	Terminated	Voluntary: Firm initiated	2016-12-07	2016-12-01
Z-0688-2017	Class III	Terminated	Voluntary: Firm initiated	2016-12-07	2016-12-01
Z-0689-2017	Class III	Terminated	Voluntary: Firm initiated	2016-12-07	2016-12-01

Product code LZO

K100866Class IIProfemur Hip System Modular NecksWrightmedicaltechnologyinc / cleared 2010-04-28

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)