MicroPort Orthopedics Inc. PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK
Brand
MicroPort Orthopedics Inc.
Lot Codes / Batch Numbers
Catalog Number(s): PHAPCLS7, Lot Number(s): 1903727, Expiration Date: 11/24/2029, UDI/DI Number: 00192629112773
Products Sold
Catalog Number(s): PHAPCLS7; Lot Number(s): 1903727; Expiration Date: 11/24/2029; UDI/DI Number: 00192629112773
MicroPort Orthopedics Inc. is recalling PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK due to One manufacturing lot is missing the plasma-spray coating in the proximal region of the stem body.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
One manufacturing lot is missing the plasma-spray coating in the proximal region of the stem body.
Recommended Action
Per FDA guidance
The firm sent out a recall notification to the distributors on 05/04/2022 via email. Phone calls were also made to the distributors. Additionally, the US field communication letter was mailed to the surgeon and facility in regard to the one case of implantation on May 10, 2022. The consignee letter informed the consignee to cease use and distribution of the affected product, check inventory for affected product, complete the response form, return affected product and notify affected consignees. The field surgeon letter and hospital letter informs the consignee to cease use and distribution of the affected product, monitor patients per normal protocol, return affected product and sign and return the response form.
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