FDA Medical Device Recalls (openFDA)
Exactech, Inc.: AcuMatch Hip System, Catalog Number 142-32-27
- Recall number
- Z-0577-2024
- Recalling firm
- Exactech, Inc.
- Product
- AcuMatch Hip System, Catalog Number 142-32-27
- Status
- Open, Classified
- Initiated
- 2023-11-21
- Posted
- 2024-01-18
- Terminated
- not on file
- Reason
- Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.
- Root cause
- Packaging change control
- Action
- Exactech issued an URGENT MEDICAL DEVICE RECALL notice to its direct consignees on 11/21/2023 via email. The notice explained the issue, clinical impact, and requested the removal and return of all affected products. 11/22/2023, the firm initiated the recall OUS also by email.
- Quantity
- not on file
- Distribution
- US NY, TX, IN, IL, MN, KY, VA, MD, TN, GA, NH, ME, SC, NV, FL, AR and Australia, Brazil, Chile, France, Germany, Guatemala, Italy, Japan, Korea, Slovenia, Spain, UK
- Lot, serial or model codes
- GTIN 10885862538192, Serial Numbers: A673200, A673204, A673209
- 510(k) numbers
- ["K173583"]
- PMA numbers
- not on file
- Product code
- OQI
- 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