Xiros Plc 28-30 Blenheim Terrace Leeds United Kingdom Neoligaments Staple Impactor, 6 mm Staple Impactor: 202-3001 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Neoligaments Staple Impactor, 6 mm Staple Impactor: 202-3001
Brand
Xiros Plc 28-30 Blenheim Terrace Leeds United Kingdom
Lot Codes / Batch Numbers
N/A
Products Sold
N/A
Xiros Plc 28-30 Blenheim Terrace Leeds United Kingdom is recalling Neoligaments Staple Impactor, 6 mm Staple Impactor: 202-3001 due to The impactors are being recalled for modification so that they can be disassembled fully for cleaning and sterilization, on suspicion that the assembl. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The impactors are being recalled for modification so that they can be disassembled fully for cleaning and sterilization, on suspicion that the assembled items retain contamination after cleaning and may not be effectively sterilized by the recommended hospital sterilization cycles.
Recommended Action
Per FDA guidance
Customer recall notifications included: a) Telephone notification to highest volume users b) Recall letters were sent via certified mail to all customers June 1, 2006. Customers were instructed to cease using immediately and return the Impactors to Tapco. The customers were instructed to call the firm for a return authorization number. Modified loaner Impactors will be made available to customers as soon as possible.
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