{ "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": "2026-08-13", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "123126", "product_res_number": "Z-0352-2014", "event_date_initiated": "2013-10-17", "event_date_posted": "2013-11-20", "recall_status": "Terminated", "event_date_terminated": "2014-04-24", "res_event_number": "66721", "product_code": "BSZ", "k_numbers": [ "K003251", "K010850" ], "product_description": "CAS I/II Absorbers that are parts of the BleaseSirius Anesthesia Workstation, the BleaseFocus Anesthesia Workstation with the following part numbers: 12200900; 12200901; 12200902; 12200903; 14200100, and service kits part number 050-0659-00 and 050-0901-00. \n\nBleaseFocus Anesthesia Workstation: The Blease Frontline Plus Range, Anesthesia Machines are intended for use in the hospital environment and locations not requiring portability. It may be used for the delivery of oxygen, air and nitrous oxide in a controlled manner to various patient breathing circuits with or without the use of a mechanical ventilator, and may be used for the delivery of anesthetic vapor by use of a dismountable vaporizer. This device is intended for use only by a suitably qualified physician. BleaseSirius Anesthesia Workstation: The Spacelabs BleaseSirius Anesthesia Workstation is intended for use in the hospital environment and operating room. It may be used for the delivery of oxygen, air and nitrous oxide in a controlled manner to various patient breathing circuits with or without the use of mechanical ventilator, and may be used for the delivery of anesthetic vapor by use of a dismountable vaporizer. The device is intended for use only by a suitably qualified physician.", "code_info": "SERIAL NUMBERS IN THE US:  ABSO-001754, ABSO-004081, ABSO-100111, ABSO-100112, ABSO-100113, ABSO-100114, ABSO-100117, ABSO-100120, ABSO-100121, ABSO-100122, ABSO-100123, ABSO-100124, ABSO-100125, ABSO-100126, ABSO-100127, ABSO-100128, ABSO-100132, ABSO-100134, and ABSO-100135.   SERIAL NUMBERS INTERNATIONAL:  ABSO-100098, ABSO-100099, abso-100100, ABSO-100101, abso-100102, ABSO-100103, abso-100104, abso-100105, abso-100106, ABSO-100107, ABSO-100108, ABSO-100109, ABSO-100110, ABSO-100129, ABSO-100130, ABSO-100131, ABSO-100136, AND ABSO-100137.", "firm_fei_number": "3002807992", "recalling_firm": "Del Mar Reynolds Medical, Ltd.", "address_1": "1-2 Harforde Ct., Foxholes 1-2 Harforde Ct. Foxholes Business Park", "city": "Hertford", "country": "United Kingdom", "additional_info_contact": "800-522-7025", "reason_for_recall": "Spacelabs Healthcare Ltd. of United Kingdom recalls , and Service Kits, Part Number 050-0659-00 and 050-0901-00. The Bag to-Vent switch in CAS I/II Absorbers may fail due to loose fastening hardware in an absorber.", "root_cause_description": "Process control", "action": "Spacelabs Healthcare sent an Urgent Medical Device Correction letter dated November 1, 2013, to all affected customers. \nSpacelabs Healthcare also sent a customer letter (translated as necessary) to all international subsidiaries and distributors of record via e-mail on November 6, 2013. \nThe letter informed customers of a potential defect in CAS I/II Absorber products employed in the Spacelabs Healthcare BleaseSirius Anesthesia Workstation, and Service Kits, Part Number 050-0659-00 and 050-0901-00.\nThe Bag-to-Vent switch in CAS I/II Absorbers may fail. In the worst case, this would result in a large leak from the absorber circuit and could impede the ability to provide ventilation.\nCustomers were instructed to immediately advise their staff of the problem. Customers with questions were instructed to contact Spacelabs Healthcare at 1-800-522-7025 and select 2 for Technical Support.\nFor questions regarding this recall call 800-522-7025.", "product_quantity": "37 units (19 in the US and 18 International)", "distribution_pattern": "Worldwide Distribution - USA (nationwide) including Oklahoma and North Carolina and Internationally to Libyan Arab Jamahiriya, Finland, Jordan, Mexico, Papua New Guinea, and Taiwan.", "openfda": { "k_number": [ "K170872", "K790456", "K042607", "K770554", "K112114", "K993410", "K032803", "K854213", "K151570", "K921742", "K800801", "K101439", "K122445", "K973896", "K844421", "K903135", "K965160", "K830159", "K120075", "K072884", "K981845", "K000995", "K923519", "K791530", "K103035", "K884879", "K030939", "K945722", "K935546", "K771479", "K971030", "K963481", "K003251", "K903991", "K131945", "K803052", "K191027", "K802591", "K974193", "K171292", "K841370", "K882489", "K760228", "K893780", "K973971", "K083098", "K050626", "K830680", "K033026", "K041622", "K060193", "K071142", "K000706", "K963994", "K850648", "K945234", "K031400", "K853435", "K042419", "K901119", "K251352", "K844849", "K970163", "K853139", "K930492", "K102389", "K844563", "K890410", "K901713", "K132530", "K864590", "K062388", "K051629", "K900329", "K133958", "K011404", "K201957", "K844008", "K971425", "K864806", "K213867", "K973949", "K933285", "K042154", "K252746", "K062155", "K132903", "K864589", "K102471", "K946127", "K983635", "K905635", "K822218", "K001727", "K833335", "K253330", "K980553", "K830161", "K863207", "K945463", "K833147", "K110213", "K884991", "K982137", "K884802", "K050055", "K131790", "K894309", "K081844", "K900937", "K122063", "K902962", "K872178", "K123125", "K864447", "K801100", "K830160", "K003579", "K000859", "K061102", "K052335", "K071097", "K033498", "K230931", "K040743", "K913791", "K771057", "K992421", "K923172", "K001488", "K113633", "K833151", "K080175", "K151954", "K781492", "K801102", "K022031", "K771989", "K092864", "K972848", "K081447", "K930351", "K841274", "K862831", "K061609", "K171311", "K142552", "K003663", "K852175", "K143530", "K172045", "K965041", "K072420", "K140264", "K864644", "K041430", "K042086", "K083413", "K123211", "K973985", "K133886", "K081941", "K801103", "K840356", "K090892", "K901117", "K160665", "K050883", "K934669", "K001315", "K102182", "K073707", "K030624", "K012446", "K920944", "K001988", "K050676", "K861170", "K900328", "K851621", "K862085", "K855022", "K090233", "K844012", "K925580", "K112722", "K981530", "K010613", "K875350" ], "registration_number": [ "", "3022543477", "3003589956", "3014579161", "3005783425", "3010157426", "2221819", "3001104093", "8043316", "3035111606", "3013188547", "9617604", "9710602", "1066270", "3021559257", "9610531", "3009129579", "3009156722", "1054713", "2020813", "9611295", "3016618143", "1530958", "8010042", "2518157", "1066427", "2112667", "1000122786", "3005803793", "3007603826", "3000126629", "3007238566", "3010703925", "9611500" ], "fei_number": [ "", "3022543477", "3002808128", "3003589956", "3002807907", "3014579161", "3005783425", "3010157426", "2221819", "3001104093", "3035111606", "3000957797", "3013188547", "1000639866", "3007513035", "3003513129", "3021559257", "3009129579", "3009156722", "3023530182", "2020813", "3003319165", "3016618143", "3002807992", "2518157", "2112667", "1000122786", "3005803793", "3007603826", "3000126629", "3007238566", "3002558692", "1000114111", "3010703925" ], "device_name": "Gas-Machine, Anesthesia", "medical_specialty_description": "Anesthesiology", "regulation_number": "868.5160", "device_class": "2" } } ] }