FDA Device recall Z-3020-2020
Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 22 mm
- FDA Device
- Class II
- terminated
- Published 2020-10-07
On 2020-10-07 the FDA classified a Class II recall of Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 22 mm by Exactech, citing exactech is recalling the Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit, because it may contain a incorrect length screw.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3020-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-08-24 |
| Published | 2020-10-07 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Exactech |
| Distribution | AR, AZ, CA, CO, FL, GA, HI, ID, IL, IN, KS, KY, LA, ME, MN, NY, OH, SC, TN, TX, VA, WA, WI |
Product
Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 22 mm.
Reason
Exactech is recalling the Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit, because it may contain a incorrect length screw.
Identifiers
| code_info | Catalog Number: 320-20-22 Serial Numbers: S071601, S071602, S071603, S071604, S071605, S071606, S071607, S071608, S07…Catalog Number: 320-20-22 Serial Numbers: S071601, S071602, S071603, S071604, S071605, S071606, S071607, S071608, S071609, S071610, S071611, S071612, S071613, S071614, S071616, S071617, S071618, S071619, S071620, S071621, S071622, S071623, S071624, S071625, S071626, S071627, S071628, S071629, S071630, S071631, S071632, S071633, S071634, S071635, S071636, S071637, S071638, S071639, S071640, S071641, S071642, S071643, S071644, s071645, S071646, S071647, S071648, S071649, S071650, S071651, S071652, S071653, S071654, S071655, S071656, S071657, S071658, S071659, S071660, S071661, S071662, S071663, S071664, S071665, S071666, S071668, S071669, S071670, S071671, S071672, S071673, S071674, S071675, S071676, S071678, S071679, S071680, S071681, S071682, S071683, S071684, S071685, S071686, S071687, S071688, S071689, S071690, S071691, S071692, S071693, S071694, S071695, S071696, S071697, S071698, S071700, S071701, S071702, S071703, S071704, S071705, S071706, S071707, S071708, S071709, S071710, S0 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3020-2020%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.