FDA recall Z-0328-2020

Product

Various fixation systems and accessories, Item Nos. 00224000916 00224000918 00224000920 00224000922 00224000924 00224000926 00224000928 00224000930 00224000932 00224000934 00224000936 00224000938 00224000940 00224000942 00224000944 00224000946 00224001014 00224001016 00224001018 00224001020 00224001022 00224001024 00224001026 00224001028 00224001030 00224001032 00224001034 00224001036 00224001038 00224001040 00224001042 00224001046 00224001048 00224001114 00224001116 00224001118 00224001120 00224001122 00224001124 00224001126 00224001128 00224001130 00224001132 00224001134 00224001136 00224001138 00224001140 00224001142 00224001144 00224001146 00224001214 00224001216 00224001218 00224001220 00224001222 00224001224 00224001226 00224001228 00224001230 00224001232 00224001234 00224001236 00224001238 00224001240 00224001242 00224001244 00224001246 00224001248 00224001314 00224001316 00224001318 00224001320 00224001322

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-0328-2020