Wright Medical Technology Inc Alumina ceramic liner for acetabular shell. This is part of the Transcend ceramic-on-ceramic total hip system. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Alumina ceramic liner for acetabular shell. This is part of the Transcend ceramic-on-ceramic total hip system.
Brand
Wright Medical Technology Inc
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Part No. Lot Serial No. 73003258 070A122950 71002846 101A147607 72003252 101A147579 71002846 01214750 73003258 020A116075 73003258 101A147616 71002846 101A147609 71002846 01214749 72003252 01214581 72003252 01215268 73003258 101A147617 73003258 01214576 74003664 101A147618 72003252 101A147580 71002846 048A080430 72003252 0124580 71002846 01214751 74003664 061A136523 72003252 119A112057 73003258 01214575 71002846 031A139399 72003252 101A147577 72003252 01214582 72003252 101A147578 71002846 039A100609 72003252 081A145884
Wright Medical Technology Inc is recalling Alumina ceramic liner for acetabular shell. This is part of the Transcend ceramic-on-ceramic total due to Wright Medical commercially distributed Transcend alumina acetabular shell liners lacking the required process validation.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Wright Medical commercially distributed Transcend alumina acetabular shell liners lacking the required process validation.
Recommended Action
Per FDA guidance
Distributors returned thier stock after May 8, 2003
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