Skip to the content

FDA Medical Device Recalls (openFDA)

Ethicon Endo-Surgery: ABSOLOK Extra Absorbable Ligating Clip cartridges, medium/large, code AP300. Ten cartridges are packaged per box.

Recall number
Z-0656-05
Recalling firm
Ethicon Endo-Surgery
Product
ABSOLOK Extra Absorbable Ligating Clip cartridges, medium/large, code AP300. Ten cartridges are packaged per box.
Status
Terminated
Initiated
2005-02-28
Posted
2005-03-25
Terminated
2007-02-21
Reason
The product is being recalled because the possibility exists that the sterility of the ligating clips may have been compromised by a tear in the ABSOLOK Extra packaging.
Root cause
Other
Action
The recalling firm sent a letter, dated 2/28/05 to consignees.
Quantity
15,462 boxes.
Distribution
The product was distributed throughout the United States and to foreign customers located in Saudi Arabia, Egypt, United Kingdom, Germany, France, Republic of Panama, Turkey, Hong Kong, Taiwan, Puerto Rico, Spain, Japan, China, Republic of Singapore, Argentina, Italy, New Zealand, Australia, Canada, Czech Republic, Sweden, Portugal, Slovenia, Poland, Hungary, and the United Arab Emirate.
Lot, serial or model codes
Lot: SK2037, exp. date 07/08; SK2055, exp. date 07/08; SL2104, exp. date 07/08; SL2118, exp. date 07/08; SL2445, exp. date 07/08; SM2135, exp. date 07/08; SP2530, exp. date 07/08; SP2711, exp. date 07/08; TA2840, exp. date 01/09; TB2335, exp. date 01/09; TC7957, exp. date 01/09; TD2044, exp. date 01/09; TD2280, exp. date 01/09; TD2664, exp. date 01/09; TD2938, exp. date 01/09; TE7512, exp. date 01/09; TG7713, exp. date 01/09; TG7825, exp. date 01/09; TG7936, exp. date 01/09; TK2477, exp. date 07/09; TK7626, exp. date 07/09; TL2169, exp. date 07/09; TL7265, exp. date 07/09; TP7279, exp. date 07/09; UA2517, exp. date 01/10; UA2747, exp. date 01/10; UA2932, exp. date 01/10; and UA7902, exp. date 01/10.
510(k) numbers
["K812323"]
PMA numbers
not on file
Product code
FZP
Firm FEI
1527736
Firm city
Cincinnati
Firm state
OH
Firm country
not on file

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

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

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

Search this register