FDA Device recall Z-2584-2014

Natural-Knee System Patella Bushings Orthopedic surgical instrument

FDA Device
Class II
terminated
Published 2014-09-10

On 2014-09-10 the FDA classified a Class II recall of Natural-Knee System Patella Bushings Orthopedic surgical instrument by Zimmer, citing zimmer received a trend of complaints indicating corrosion of product.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2584-2014
Classification	Class II
Status	terminated
Initiated	2014-07-10
Published	2014-09-10
Last updated	2026-09-13 11:53 UTC
Company	Zimmer
Distribution	n/a

Product

Natural-Knee System Patella Bushings Orthopedic surgical instrument. Part Number: 6290-00-703. Per the Natural-Knee II Primary System Surgical Technique, the patellar bushing is placed on the cut surface of the patella and used as a guide for the matching size patella cutter.

Reason

Zimmer received a trend of complaints indicating corrosion of product.

Identifiers

code_info	Part Number: 6290-00-703. Lots Manufactured by Zimmer: 1324204, 1346689, 1361954, 1371127, 1374460, 1382191, 138607… Part Number: 6290-00-703. Lots Manufactured by Zimmer: 1324204, 1346689, 1361954, 1371127, 1374460, 1382191, 1386076, 1388163, 1421648, 1440890, 1441119, 1476227, 1476229, 1493832, 1493841, 1516853, 1530324, 1549264, 1549388, 1554288, 1554290, 1560754, 1563440, 1598691, 1598692, 1598693, 1598695, 1601605, 1606099, 1606510, 170675, 172016, 173342-09, 173342-10 , 173342-3 , 173342-5, 173342-9 , 601804, 60278820, 60310873, 60426582, 60541727, 60621363, 60641020, 60728521, 60763272, 60933532, 60936986, 60946365, 60947926, 60954309, 60961655, 60964904, 60970610, 60978734, 60998043, 61004755, 61019426, 61025143, 61037534, 61092670, 61092673, 61092674, 61099693, 61188779, 61208208, 61244656, 61444749, 61588176, 61626531, 61815323, 618303, 61910780, 62007198, 62159771, 62238171, 62298008, 62495684, 672559, 691440, 739625, 751350, 784259, 784516, 786652, 791148, 795930, 802251, 803806, 825358-2, 831816-1, 863218-1, 865553, 866726, & 869004. Lots Manufactured by Centerpulse: 9878, 11486

code_info

Part Number: 6290-00-703. Lots Manufactured by Zimmer: 1324204, 1346689, 1361954, 1371127, 1374460, 1382191, 138607…

Part Number: 6290-00-703. Lots Manufactured by Zimmer: 1324204, 1346689, 1361954, 1371127, 1374460, 1382191, 1386076, 1388163, 1421648, 1440890, 1441119, 1476227, 1476229, 1493832, 1493841, 1516853, 1530324, 1549264, 1549388, 1554288, 1554290, 1560754, 1563440, 1598691, 1598692, 1598693, 1598695, 1601605, 1606099, 1606510, 170675, 172016, 173342-09, 173342-10 , 173342-3 , 173342-5, 173342-9 , 601804, 60278820, 60310873, 60426582, 60541727, 60621363, 60641020, 60728521, 60763272, 60933532, 60936986, 60946365, 60947926, 60954309, 60961655, 60964904, 60970610, 60978734, 60998043, 61004755, 61019426, 61025143, 61037534, 61092670, 61092673, 61092674, 61099693, 61188779, 61208208, 61244656, 61444749, 61588176, 61626531, 61815323, 618303, 61910780, 62007198, 62159771, 62238171, 62298008, 62495684, 672559, 691440, 739625, 751350, 784259, 784516, 786652, 791148, 795930, 802251, 803806, 825358-2, 831816-1, 863218-1, 865553, 866726, & 869004. Lots Manufactured by Centerpulse: 9878, 11486

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2584-2014%22

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