FDA Medical Device Recalls (openFDA)
Exactech, Inc.: Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 18 mm.
- Recall number
- Z-3019-2020
- Recalling firm
- Exactech, Inc.
- Product
- Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 18 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
- 125 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: 320-20-18 Serial Numbers: S072858, S072859, S072860, S072861, S072862, S072863, S072864, S072865, S072866, S072867, S072868, S072869, S072870, S072871, S072872, S072873, S072874, S072875, S072876, S072877, S072878, S072879, S072880, S072881, S072882, S072883, S072884, S072885, S072886, S072887, S072888, S072889, S072890, S072891, S072892, S072893, S072894, S072895, S072896, S072897, S072898, S072899, S072900, S072901, S072902, S072903, S072905,S072906, S072907, S072908, S072909, S072910, S072923, S072924, S072925, S072926, S072927, S072928, S072929, S072930, S072931, S072932, S072933, S072934, S072935, S072936, S072937, S072938, S072939, S072940, S072941, S072942, S072943, S072944, S072945, S072946, S072947, S072948, S072949, S072950, S072951, S072952, S072953, S072954, S072955, S072956, S072957, S072959, S072962, S072963, S072964, S072965, S072966, S072969, S072970, S072971, S072972, S072973, S072974, S072975, S072976, S072977, S072978, S072979, S072980, S072981, S072982, S072983, S072984, S072985, S072986, S072987, S072988, S072989, S072990, S072991, S072992, S072993, S072994, S072995, S072996, S072997, S072998, S072999.
- 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