{ "meta": { "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.", "terms": "https://open.fda.gov/terms/", "license": "https://open.fda.gov/license/", "last_updated": "2026-08-20", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "37841", "product_res_number": "Z-0656-05", "event_date_initiated": "2005-02-28", "event_date_posted": "2005-03-25", "recall_status": "Terminated", "event_date_terminated": "2007-02-21", "res_event_number": "31351", "product_code": "FZP", "k_numbers": [ "K812323" ], "product_description": "ABSOLOK Extra Absorbable Ligating Clip cartridges, medium/large, code AP300. Ten cartridges are packaged per box.", "code_info": "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.", "firm_fei_number": "1527736", "recalling_firm": "Ethicon Endo-Surgery", "address_1": "4545 Creek Rd", "city": "Cincinnati", "state": "OH", "postal_code": "45242-2803", "additional_info_contact": "Carol Montandon\n513-337-3419", "reason_for_recall": "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_description": "Other", "action": "The recalling firm sent a letter, dated 2/28/05 to consignees.", "product_quantity": "15,462 boxes.", "distribution_pattern": "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.", "openfda": { "k_number": [ "K032238", "K150840", "K021407", "K993424", "K841549", "K053252", "K040821", "K030311", "K071406", "K873309", "K232313", "K933887", "K143598", "K081031", "K091060", "K050344", "K151943", "K964470", "K982944", 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