FDA Device recall Z-1950-2016
POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM X 10MM- 00587806535 POROUS PATELLA 38MM X 10MM - 00587806538 POROUS PATELLA 41…
- FDA Device
- Class II
- terminated
- Published 2016-06-22
On 2016-06-22 the FDA classified a Class II recall of POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM X 10MM- 00587806535 POROUS PATELLA 38MM X 10MM - 00587806538 POROUS PATELLA 41… by Zimmer Trabecular Metal Technology, citing zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouch….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1950-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-04-15 |
| Published | 2016-06-22 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Trabecular Metal Technology |
| Distribution | US |
Product
POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM X 10MM- 00587806535 POROUS PATELLA 38MM X 10MM - 00587806538 POROUS PATELLA 41MM X 10MM - 00587806541
Reason
Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
Identifiers
| code_info | POROUS PATELLA 32MM X 10MM 61728647 61762587 62028703 62082384 61998061 61728648 61781040 62028701 62082387 61998065…POROUS PATELLA 32MM X 10MM 61728647 61762587 62028703 62082384 61998061 61728648 61781040 62028701 62082387 61998065 61762578 61781037 62028702 62100771 62003279 61762581 61781039 62028705 62100774 62003280 61762584 61796452 62051894 62100773 61998062 61762585 61796458 62051896 62100775 61998064 61770640 61770641 62051895 62100777 62003281 61770642 61796459 62109088 62109087 62003282 61762579 61781036 62109089 62100768 62003283 61762580 61770638 62100770 62100769 62007635 61762582 61781038 62109090 62100772 62007636 61762583 61796451 62119906 62100776 61874756 61770639 61796460 62119907 62109086 61874758 61890052 61910583 61890055 61914846 61878840 61890053 61910584 61890054 61914845 61878841 61890056 61896662 61910581 61830190 61878844 61844395 61890050 61910582 61830189 61890058 61914849 61830191 61844393 62007641 62082386 61914848 61850552 61850551 62022120 62082388 61946320 61874757 61850549 62022121 62082383 61952743 61878842 61850553 62022123 62082379 619771 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1950-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.