Wright Medical Technology, Inc. WRIGHT EVOLVE Proline Head, Size: +2, OD: 20mm, REF 496H220 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
WRIGHT EVOLVE Proline Head, Size: +2, OD: 20mm, REF 496H220
Brand
Wright Medical Technology, Inc.
Lot Codes / Batch Numbers
Lot Code 1633010
Products Sold
Lot Code 1633010
Wright Medical Technology, Inc. is recalling WRIGHT EVOLVE Proline Head, Size: +2, OD: 20mm, REF 496H220 due to Two lots of EVOLVE Modular Radial Head could have the wrong size product in the package. Both the label and laser marking are incorrect on the affect. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Two lots of EVOLVE Modular Radial Head could have the wrong size product in the package. Both the label and laser marking are incorrect on the affected product.
Recommended Action
Per FDA guidance
The firm initiated the recall by email and letter on 12/27/2019. The notices requests the following actions: Immediately quarantine all recalled products they have and return all affected product to Wright Medical as soon as possible. If they have further distributed the affected product, we are asking them to notify the applicable parties at once about this recall. They may copy and distribute the notification letter and Wright Medical will work directly with them to collect the recalled items.
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