Stryker Howmedica Osteonics Corp. T2 System, Condyle Screw Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
T2 System, Condyle Screw
Brand
Stryker Howmedica Osteonics Corp.
Lot Codes / Batch Numbers
Catalog No. 1895-5085S to 1895-5120S
Products Sold
Catalog No. 1895-5085S to 1895-5120S
Stryker Howmedica Osteonics Corp. is recalling T2 System, Condyle Screw due to Stryker Orthopaedics was informed by the manufacturer, that in some instances, the sterile blister package of the referenced G/K, T2 condyle and some . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Stryker Orthopaedics was informed by the manufacturer, that in some instances, the sterile blister package of the referenced G/K, T2 condyle and some S2 screw products may become damaged during shipping and handling which may result in a potential breach of the sterile barrier.
Recommended Action
Per FDA guidance
The product recall will extend to all branches.agencies and hospitals that have received the product.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026