Depuy Mitek, a Johnson & Johnson Co. Depuy Mitek Bioknotless Anchor with Ethibond Suture Ref No. 212728 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Depuy Mitek Bioknotless Anchor with Ethibond Suture Ref No. 212728
Brand
Depuy Mitek, a Johnson & Johnson Co.
Lot Codes / Batch Numbers
Lot Number: 1358481 Exp Date: Nov 2008
Products Sold
Lot Number: 1358481 Exp Date: Nov 2008
Depuy Mitek, a Johnson & Johnson Co. is recalling Depuy Mitek Bioknotless Anchor with Ethibond Suture Ref No. 212728 due to The inserter shafts bend, as they were manufactured with a different stainless steel than specified.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The inserter shafts bend, as they were manufactured with a different stainless steel than specified.
Recommended Action
Per FDA guidance
Depuy Mitek notified consignees by letter dated 2/17/06 to request accounts return devices.
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