Ossur North America Inc VSP Shock Module (as part of a prosthetic foot). Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
VSP Shock Module (as part of a prosthetic foot).
Brand
Ossur North America Inc
Lot Codes / Batch Numbers
RFL0001, RFL00008, RFL50006, RFX00001, RFX00002, RFX00012.
Products Sold
RFL0001, RFL00008, RFL50006, RFX00001, RFX00002, RFX00012.
Ossur North America Inc is recalling VSP Shock Module (as part of a prosthetic foot). due to Flawed shock module might cause breakage causing patient to fall.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Flawed shock module might cause breakage causing patient to fall.
Recommended Action
Per FDA guidance
Firm will be contacting customers and patients to replace the defective components. Contact will be made by mail and by phone.
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