FDA Device recall Z-1031-2017
AcuMatch A-Series Connexion GXL Enhanced Polyethylene Acetabular Liner, 15, +5 mm Lateralized, 36 mm I.D., Size J
- FDA Device
- Class II
- terminated
- Published 2017-01-25
On 2017-01-25 the FDA classified a Class II recall of AcuMatch A-Series Connexion GXL Enhanced Polyethylene Acetabular Liner, 15, +5 mm Lateralized, 36 mm I.D., Size J by Exactech, citing products were labeled with incorrect Global Trade Item Numbers. The GTIN on the label identifies the devices as another.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1031-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-11-07 |
| Published | 2017-01-25 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Exactech |
| Distribution | AZ, CA, CO, FL, IL, KS, MD, NJ, NY, OH, OK, TN, VA |
Product
AcuMatch A-Series Connexion GXL Enhanced Polyethylene Acetabular Liner, 15, +5 mm Lateralized, 36 mm I.D., Size J.
Reason
Products were labeled with incorrect Global Trade Item Numbers. The GTIN on the label identifies the devices as another.
Identifiers
| code_info | Serial No. 4507932-4507943; Catalog No. 138-36-29; UDI: 10885862024831 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1031-2017%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.