Datascope Corp Anestar Anesthesia Delivery System Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Anestar Anesthesia Delivery System
Brand
Datascope Corp
Lot Codes / Batch Numbers
Serial#: 4600010001, 4600010003, 4600010004, 4600010007, 4600010008, 4600010009, 4600010010, 4600010012, 4600A20017, 4600A20018, 4600A20019, 4600A20020, 4600A20021, 4600A20023, 4600A20024, 4600A30066, 4600A30067, 4600A30068, 4600A30069, 4600A30070, 4600A30071, 4600A30072, 4600A30073, 4600A30074, 4600A30075, 4600B10002, 4600B20025, 4600B20026, 4600B20027, 4600B20028, 4600B20029, 4600B20030, 4600B20031, 4600B20032, 4600B20033, 4600B20034, 4600B30076, 4600B30077, 4600B30078, 4600B30079, 4600B30080, 4600B30081, 4600B30082, 4600B30083, 4600B30084, 4600B30086, 4600C30087, 4600C30088, 4600C30089, 4600C30091, 4600C30092, 4600C30093, 4600C30094, 4600C30095, 4600C30096, 4600C30097, 4600C30098, 4600C30099, 4600D20035, 4600D20036, 4600D20037, 4600D20038, 4600D20039, 4600D20040, 4600D20041, 4600D20042, 4600D20043, 4600D20044, 4600H20045, 4600H20046, 4600H20047, 4600H20048, 4600H20049, 4600H20050, 4600H20051, 4600H20052, 4600H20053, 4600H20054, 4600I10013, 4600J20055, 4600J20056, 4600J20057, 4600J20058, 4600J20059, 4600J20060, 4600J20061, 4600J20062, 4600J20063, 4600J20064.
Products Sold
Serial#: 4600010001; 4600010003; 4600010004; 4600010007; 4600010008; 4600010009; 4600010010; 4600010012; 4600A20017; 4600A20018; 4600A20019; 4600A20020; 4600A20021; 4600A20023; 4600A20024; 4600A30066; 4600A30067; 4600A30068; 4600A30069; 4600A30070; 4600A30071; 4600A30072; 4600A30073; 4600A30074; 4600A30075; 4600B10002; 4600B20025; 4600B20026; 4600B20027; 4600B20028; 4600B20029; 4600B20030; 4600B20031; 4600B20032; 4600B20033; 4600B20034; 4600B30076; 4600B30077; 4600B30078; 4600B30079; 4600B30080; 4600B30081; 4600B30082; 4600B30083; 4600B30084; 4600B30086; 4600C30087; 4600C30088; 4600C30089; 4600C30091; 4600C30092; 4600C30093; 4600C30094; 4600C30095; 4600C30096; 4600C30097; 4600C30098; 4600C30099; 4600D20035; 4600D20036; 4600D20037; 4600D20038; 4600D20039; 4600D20040; 4600D20041; 4600D20042; 4600D20043; 4600D20044; 4600H20045; 4600H20046; 4600H20047; 4600H20048; 4600H20049; 4600H20050; 4600H20051; 4600H20052; 4600H20053; 4600H20054; 4600I10013; 4600J20055; 4600J20056; 4600J20057; 4600J20058; 4600J20059; 4600J20060; 4600J20061; 4600J20062; 4600J20063; 4600J20064.
Datascope Corp is recalling Anestar Anesthesia Delivery System due to Failure of the Anestar AC Main Power Switch. Battery should last 30 minutes, then ventilation and monitoring will fail.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Failure of the Anestar AC Main Power Switch. Battery should last 30 minutes, then ventilation and monitoring will fail.
Recommended Action
Per FDA guidance
A Field Correction action was initiated in June, 2003 and completed by the service reps in April, 2004.
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