[Recalled] Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 138-22-XX, Novation GXL 10 deg Liner, G00, 22mm ID. Orthopedic hip implant component. — Risk of edge-loading and premature pros
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 138-22-XX, Novation GXL 10 deg Liner, G00, 22mm ID. Orthopedic hip implant component. |
|---|---|
| Brand / manufacturer | Exactech, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2130-2021 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 29 June 2021 |
| EAN / barcode | 10885862024503 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Risk of edge-loading and premature prosthesis wear is possible in a specific subset of patients with certain implant configurations and surgical implant positioning.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Exactech, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.