Zimmer, Inc. PERSONA" The Personalized Knee System UC Tibial Articular Surface Provisional Left Size 3-7 CD Top; Left Size 4-11 EF Top; Left Size 7-12 GH Top; Left Size 9-12 J Top; Right Size 3-7 CD Top; Right Size 4-11 EF Top; Right Size 7-12 GH Top; and Right Size 9-12 J Top. Recall
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
PERSONA" The Personalized Knee System UC Tibial Articular Surface Provisional Left Size 3-7 CD Top; Left Size 4-11 EF Top; Left Size 7-12 GH Top; Left Size 9-12 J Top; Right Size 3-7 CD Top; Right Size 4-11 EF Top; Right Size 7-12 GH Top; and Right Size 9-12 J Top.
Brand
Zimmer, Inc.
Lot Codes / Batch Numbers
Part Numbers: 42517200410, 42517200510, 42517200610, 42517200710, 42527200410, 42527200510, 42527200610, and 42527200710. Lot numbers:62034570, 62117742, 62156315, 62187322, 62247350, 62314721, 62372409, 62381836, 62397160, 62429190, 62474906, 62551390, 62565048, 62595853, 62614781, 62700416, 62702297, 62724349, 62043548, 62055681, 62104368, 62117743, 62144794, 62165545, 62177246, 62256282, 62351288, 62356244, 62391228, 62427419, 62456268, 62506003, 62551338, 62564355, 62597762, 62614786, 62702292, 62705808, 62717332, 62055682, 62068376, 62068378, 62144795, 62152727, 62187323, 62256283, 62351289, 62356275, 62386419, 62445931, 62456266, 62558584, 62575757, 62611087, 62638672, 62698749, 62736074, 62736075, 62330130, 62563854, 62567418, 62622596, 62070845, 62102088, 62130979, 62149717, 62200303, 62240485, 62256293, 62351304, 62356605, 62391239, 62420238, 62469444, 62551099, 62581081, 62597792, 62627223, 62696849, 62715617, 62059519, 62072593, 62103263, 62110051, 62196614, 62198205, 62248171, 62351307, 62385105, 62401423, 62468266, 62558588, 62595866, 62690052, 62715613, 62072225, 62103266, 62144798, 62156319, 62209049, 62229728, 62282887, 62315140, 62356622, 62386430, 62401427, 62427062, 62428459, 62505998, 62565073, 62581864, 62627283, 62690948, 62696884, 62717330, 62398030, 62428342, 62444343, 62510048, 62515508, 62516058, and 62600154.
Products Sold
Part Numbers: 42517200410, 42517200510, 42517200610, 42517200710, 42527200410, 42527200510, 42527200610, and 42527200710. Lot numbers:62034570, 62117742, 62156315, 62187322, 62247350, 62314721, 62372409, 62381836, 62397160, 62429190, 62474906, 62551390, 62565048, 62595853, 62614781, 62700416, 62702297, 62724349, 62043548, 62055681, 62104368, 62117743, 62144794, 62165545, 62177246, 62256282, 62351288, 62356244, 62391228, 62427419, 62456268, 62506003, 62551338, 62564355, 62597762, 62614786, 62702292, 62705808, 62717332, 62055682, 62068376, 62068378, 62144795, 62152727, 62187323, 62256283, 62351289, 62356275, 62386419, 62445931, 62456266, 62558584, 62575757, 62611087, 62638672, 62698749, 62736074, 62736075, 62330130, 62563854, 62567418, 62622596, 62070845, 62102088, 62130979, 62149717, 62200303, 62240485, 62256293, 62351304, 62356605, 62391239, 62420238, 62469444, 62551099, 62581081, 62597792, 62627223, 62696849, 62715617, 62059519, 62072593, 62103263, 62110051, 62196614, 62198205, 62248171, 62351307, 62385105, 62401423, 62468266, 62558588, 62595866, 62690052, 62715613, 62072225, 62103266, 62144798, 62156319, 62209049, 62229728, 62282887, 62315140, 62356622, 62386430, 62401427, 62427062, 62428459, 62505998, 62565073, 62581864, 62627283, 62690948, 62696884, 62717330, 62398030, 62428342, 62444343, 62510048, 62515508, 62516058, and 62600154.
Zimmer, Inc. is recalling PERSONA" The Personalized Knee System UC Tibial Articular Surface Provisional Left Size 3-7 CD Top; due to Reports of breakage of the Persona Knee Trial Articular Surface Provisionals (TASPs). The Persona primary knee surgical technique has been updated. Th. This is a Class I recall, indicating a high risk of serious health consequences or death. Based on FDA medical device enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Reports of breakage of the Persona Knee Trial Articular Surface Provisionals (TASPs). The Persona primary knee surgical technique has been updated. This field action correction is to ensure that all distributors and users of this instrument are aware of the enhanced surgical techniques.
Recommended Action
Per FDA guidance
Healthcare providers and patients should stop using the device and contact the manufacturer for further instructions. Report problems to FDA MedWatch.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026