FDA Device recall Z-0577-2024
AcuMatch Hip System, Catalog Number 142-32-27
- FDA Device
- Class II
- ongoing
- Published 2023-12-27
On 2023-12-27 the FDA classified a Class II recall of AcuMatch Hip System, Catalog Number 142-32-27 by Exactech, citing exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0577-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-11-21 |
| Published | 2023-12-27 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Exactech |
| Distribution | AR, FL, GA, IL, IN, KY, MD, ME, MN, NH, NV, NY, SC, TN, TX, VA |
Product
AcuMatch Hip System, Catalog Number 142-32-27
Reason
Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.
Identifiers
| code_info | GTIN 10885862538192, Serial Numbers: A673200, A673204, A673209 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0577-2024%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.