FDA Device recall Z-1031-2018
CR-FLX POR HATCP FEM C-L MINUS CR-FLX POR HATCP FEM C-R MINUS CR-FLX POR HATCP FEM D-L MINUS CR-FLX POR HATCP FEM D-R MINUS CR-FLX POR HATC…
- FDA Device
- Class II
- terminated
- Published 2018-03-21
On 2018-03-21 the FDA classified a Class II recall of CR-FLX POR HATCP FEM C-L MINUS CR-FLX POR HATCP FEM C-R MINUS CR-FLX POR HATCP FEM D-L MINUS CR-FLX POR HATCP FEM D-R MINUS CR-FLX POR HATC… by Zimmer Biomet, citing the LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant af….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1031-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-11-29 |
| Published | 2018-03-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Biomet |
| Distribution | US |
Product
CR-FLX POR HATCP FEM C-L MINUS CR-FLX POR HATCP FEM C-R MINUS CR-FLX POR HATCP FEM D-L MINUS CR-FLX POR HATCP FEM D-R MINUS CR-FLX POR HATCP FEM E-L MINUS CR-FLX POR HATCP FEM E-R MINUS CR-FLX POR HATCP FEM F-L MINUS CR-FLX POR HATCP FEM F-R MINUS CR-FLX POR HATCP FEM G-L MINUS CR-FLX POR HATCP FEM G-R MINUS This device is indicated for patients with severe knee pain and disability
Reason
The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.
Identifiers
| code_info | 65-5952-013-05 61819644 65-5952-013-05 61855471 65-5952-013-05 11004433 65-5952-013-06 62056868 65-5952-014-05 6178…65-5952-013-05 61819644 65-5952-013-05 61855471 65-5952-013-05 11004433 65-5952-013-06 62056868 65-5952-014-05 61782591 65-5952-014-05 11003623 65-5952-014-05 61987912 65-5952-014-05 62104150 65-5952-014-06 61835232 65-5952-014-06 62038826 65-5952-014-06 62132128 65-5952-015-05 61782592 65-5952-015-05 61822359 65-5952-015-05 61857405 65-5952-015-05 11004436 65-5952-015-05 61939607 65-5952-015-05 62020177 65-5952-015-05 62046101 65-5952-015-05 62122758 65-5952-015-06 61805662 65-5952-015-06 11003505 65-5952-015-06 61848476 65-5952-015-06 11004261 65-5952-015-06 61921288 65-5952-015-06 61968654 65-5952-015-06 62001382 65-5952-015-06 62025672 65-5952-015-06 62074886 65-5952-015-06 62128161 65-5952-016-05 61801433 65-5952-016-05 61836563 65-5952-016-05 61857407 65-5952-016-05 11004258 65-5952-016-05 11004438 65-5952-016-05 61928636 65-5952-016-05 61951539 65-5952-016-05 62020178 65-5952-016-05 62056869 65-5952-016-05 62092424 65-5952-016-05 62139313 |
|---|
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-1031-2018%22
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