FDA Medical Device Recalls (openFDA)
Exactech, Inc.: The Vantage Total Ankle Tibial Insert, Fixed Bearing, Size 4, Right 10mm.
- Recall number
- Z-2926-2020
- Recalling firm
- Exactech, Inc.
- Product
- The Vantage Total Ankle Tibial Insert, Fixed Bearing, Size 4, Right 10mm.
- Status
- Open, Classified
- Initiated
- 2020-08-10
- Posted
- not on file
- Terminated
- not on file
- Reason
- The Vantage Total Ankle Tibial Insert, Fixed Bearing, Size 4, Right 10mm, were found to have a labeling error. Exactech is recalling the Vantage Total Ankle Tibial Insert, Fixed Bearing, Size 4, Right 10mm because they were found to have a labeling error. The upper right corner of the label incorrectly identifies the implant size as 3 when the implant size is 4.
- Root cause
- Error in labeling
- Action
- On August 18, 2020 Exactech sent an Urgent Product Recall Notice to all its consignees with the following instructions: -Immediately cease distribution or use of this product. -Extend this information to your accounts that may have this product in their possession. - Identify and quarantine any of the subject devices in your inventory (including loaner kits). -Complete and returned the attached Recall Inventory Response Form to Exactech via email at recalls@exac.com.
- Quantity
- 11 units
- Distribution
- Domestic: CO,FL,OK, PA. International: Chile
- Lot, serial or model codes
- Catalog Number: 350-22-44 Lot numbers: 05144883 and 05144884 Serial Numbers: 6417984, 6417989, 6417996, 6417997, 6417998, 6418002, 6418003, 6488668, 6488673,6488674,6488675.
- 510(k) numbers
- ["K152217"]
- PMA numbers
- not on file
- Product code
- HSN
- 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