FDA recall Z-0318-2020

Product

Various Hip Joint Replacement Systems, Item Nos. 00151504232 00151504432 00151504636 00151504836 00151505040 00151505240 00151505444 00151505644 00151505848 00151506048 00151506248 00151506448 00151506648 00400500060 00401000038 00401000040 00401000041 00401000042 00401000043 00401000044 00401000045 00401000046 00401000047 00401000048 00401000049 00401000050 00401000051 00401000052 00401000053 00401000054 00401000055 00402100857 00402100863 00402101243 00402101244 00402200040 00402200042 00402200051 00402200057 00408801106 00408801206 00408801226 00408801236 00408801306 00408801326 00408801336 00408801356 00408801376 00408801406 00408801426 00408801436 00408801456 00408801476 00408801506 00408801526 00408801536 00408801556 00408801576 00408801606 00408801626 00408801636 00408801656 00408801706 00408801806 00455500700 00455501001 00455502000 00455502001 00455503000 00455503001 00455504001 00500103800 00500103900 00

Reason for recall

Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

Distribution

Distributed nationwide.

Key facts

Status

Terminated

Initiation date

2019-10-10

Report date

2019-11-13

Termination date

2020-05-19

Voluntary/Mandated

Voluntary: Firm initiated

Location

Warsaw, IN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0318-2020