[Recalled] iTotal Posterior Stabilized (PS) Knee Replacement System, Catalog Number TPS-111-1111 - 020102 — The labeling of the boxes and sterile pouches did not match the contents | FDA 2019-01-04
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | iTotal Posterior Stabilized (PS) Knee Replacement System, Catalog Number TPS-111-1111 - 020102 |
|---|---|
| Brand / manufacturer | Conformis, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1079-2019 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 04 January 2019 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The labeling of the boxes and sterile pouches did not match the contents.
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 Conformis, 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.