FDA Medical Device Recalls (openFDA)
Exactech, Inc.: Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 22 mm.
- Recall number
- Z-3020-2020
- Recalling firm
- Exactech, Inc.
- Product
- Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 22 mm.
- Status
- Terminated
- Initiated
- 2020-08-24
- Posted
- not on file
- Terminated
- 2023-05-01
- Reason
- Exactech is recalling the Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit, because it may contain a incorrect length screw.
- Root cause
- Labeling Change Control
- Action
- On 8/24/2020 the firm provided a letter to their consignees with the following instructions: In order to comply with applicable regulations and Exactech policies: " Immediately cease distribution or use of this product. " Extend this information to your accounts that may have this product in their possesrion. " Identify and quarantine any of the subject devices in your inventory (including loaer kits). " Complete and return the attached Recall Inventory Response Form to Exactech via email a recalls@exac.com.
- Quantity
- 149 devices
- Distribution
- Domestic Distribution: KS, CA, AR, NY, OH, IL, WI, AZ, LA, KY, VA, IN, TX, HI, MN, FL, TN, GA, ID, ME, CO, WA, SC. International Distribution: Austria, Australia, Germany, France, Spain, Italy, Japan, United Kingdom, Luxembourg, Netherlands, South Africa.
- Lot, serial or model codes
- 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, S071711, S071712, S071713, S071714, S071715, S071716, S071717, S071718, S071719, S071720, S071721, S071724, S071725, S071726, S071727, S071728, S071729, S071730, S071731, S071732, S071733, S071734, S071735, S071736, S071737, S071738, S071739, S071740, S071741, S071742, S071743, S071744, S071745, S071747, S071748, S071749, S071750, S071751, S071752, S071753, S071754, S071755, S071756, S071757, S071758, S071759, S071760, S071761, S071762, S071763, S071765, S071766, S071767, S071768, S071769, S071770, S071771, S071772, S071773, S071774, S071775, S071776, S071777, S071778, S071781, S071782, S071783, S071784, S071785, S071786, S071787, S071788, S071789, S071790, S071791, S071792, S071793, S071794, S071795, S071796, S071797, S071798, S071799, S071800.
- 510(k) numbers
- ["K063569"]
- PMA numbers
- not on file
- Product code
- PHX
- Firm FEI
- 1038671
- Firm city
- Gainesville
- Firm state
- FL
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28