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FDA Medical Device Recalls (openFDA)

Xiros Plc: Neoligaments Staple Impactor, 6 mm Staple Impactor: 202-3001

Recall number
Z-1500-06
Recalling firm
Xiros Plc
Product
Neoligaments Staple Impactor, 6 mm Staple Impactor: 202-3001
Status
Terminated
Initiated
2006-05-17
Posted
2006-09-13
Terminated
2012-09-14
Reason
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.
Root cause
Other
Action
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.
Quantity
89
Distribution
Nationwide & Worldwide, including Spain, Japan, UAE, Italy, Germany
Lot, serial or model codes
N/A
510(k) numbers
not on file
PMA numbers
not on file
Product code
HXJ
Firm FEI
3013299874
Firm city
Leeds
Firm state
not on file
Firm country
United Kingdom

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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