Medi Manufacturing Inc Medipro OP4 Prosthetic Knee Joint (external for prosthesis, not implant). Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medipro OP4 Prosthetic Knee Joint (external for prosthesis, not implant).
Brand
Medi Manufacturing Inc
Lot Codes / Batch Numbers
Serial numbers 22509, 24208, 2326D, 2334C, 2337F, 2339H, 2341A 2342B
Products Sold
Serial numbers 22509, 24208, 2326D, 2334C, 2337F, 2339H, 2341A 2342B
Medi Manufacturing Inc is recalling Medipro OP4 Prosthetic Knee Joint (external for prosthesis, not implant). due to Joints contain a component manufactured with an alloy that may not comply with manufacturer's specifications.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Joints contain a component manufactured with an alloy that may not comply with manufacturer's specifications.
Recommended Action
Per FDA guidance
Each consignee was contacted by phone on 8/11/2006. A follow up letter was sent to consignees on 8/11/2006 providing details on who to contact and how to return the affected devices for replacement. A self addressed, stamped response form was included to be completed and returned to Medi.
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