Datascope Corp Anestar and Anestar Plus Anesthesia System. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Anestar and Anestar Plus Anesthesia System.
Brand
Datascope Corp
Lot Codes / Batch Numbers
Serial Numbers starting with 4600: A51083, C51104, C51116, C51117, C51120, C51121, C51125, E41025, G30143, L41062, L41063, L41064, L41065, L41071, L41075, 010001, 010002, 010008, 010010, A20024, A51076, A51077, A51078, A51081, A51084, B20027, B30076, B30077, B30078, B30081, B30082, B30083, B41005, B51087, B51088, B51089, B51092, B51096, C30087, C30092, C30093, C30094, C30095, C30096, C30097, C30098, C30099, C30102, C41014, C41015, C41017, C41020, C51114, C51118, D20035, D20036, D20037, D20038, D20042, D20043, D20044, D30100, D30101, D30103, D30104, D30105, D30106, D30107, D30108, D30109, E30112, E30113, E30115, E30116, E30117, E30118, E41029, F30120, F30128, F30129, F30131, F30132, F30133, F30134, F30135, G30136, G30137, G30138, G30139, G30140, G30142, H20045, H20047, H20051, H20052, I10010, I41031, I41035, I41036, I41038, I41041, I41042, I41043, I41044, I41045, I41046, I41047, I41048, I41049, I41050, J20055, J20056, J20057, J20059, J20060, J20061, J20063, J20064, K41057, L41066, L41073, A20018, A20023, A30069, A30070, B20026, B20028, B20030, B30084, B30086, C41031, C41018, D20014, I41034, I41037, K41060, L30162, L41068, C51101, C51103, C51111, C51113, D51131, F30122US, F30127, H30149, I41033, I41039, I41040, 010007, E30114, H30144, H30145, H30146, H30147, H30148, H30150, H30151, H30152, H30153, H30155, A30066, A30067, A30071, A51080, A51082, A51085, B41002, B51086, B51090, B51097, C41011, C41061, C41091, C51105, C51108, C51115, C51123, D51127, D51129, D51132, D51135, E41022, E41023, E41024, E41026, F30130, H20048, I41032, K41051, K41052, K41053, K41054, K41059, L41069, A51079, B41004, B41009, A30072, A30073, A30074, A30075, D20039, D20040, E30119, H30154, 010012, A20020, A20034, K41055, K41056, K41058, L30156, L30157, L30159, L30160, L30161, L41067, L41070, L41074, A30068, B51091, B51093, B51094, B51095, C30088, C30089, C30090, C30091, D10005, E41021, E41027, E41028, E41030, L30163, L30167, B51098, C51112, B20032, D51126, D51130, D51133, D51134, L30164, L30166, F30121, F30123, A20015, A20016, A20022, B10001, B20029, B20031, B20033, B30079, B30080, B41001, B41003, B41006, B41007, B41008, B41010, C51102, C51107, C51109, C51110, F30124, F30125, F30126, G30141, H20046, H20049, H20050, H20053, H20054, I10008, I10013, J20058, J20062, L30158, L40161, A20021, L41072. Serial Numbers starting with AF0: 1040-L5, 1045-A6, 1043-L5, 1029-K5, 1037-L5, 1005-I5, 1032-K5, 1036-L5, 1035-L5, 1034-L5, 1033-L5, 1032-L5, 1031-K5, 1030-K5, 1028-K5, 1027-K5, 1026-K5, 1025-K5, 1024-K5, 1023-K5, 1022-K5, 1021-K5, 1020-K5, 1019-K5, 1018-K5, 1017-K5, 1016-K5, 1015-K5, 1014-J5, 1013-J5, 1012-J5, 1011-J5, 1009-I5, 1008-I5, 1007-I5, 1004-I5, 1003-I5, 1001-I5, 1055-A6, 1051-A6, 1048-A6, 1046-A6, 1042-L5, 1010-I5, 1044-A6, 1041-L5, 1038-L5, 1006-I5, 1053-A6, 1052-A6, 1049-A6, 1047-A6, 1039-L5.
Products Sold
Serial Numbers starting with 4600: A51083; C51104; C51116; C51117; C51120; C51121; C51125; E41025; G30143; L41062; L41063; L41064; L41065; L41071; L41075; 010001; 010002; 010008; 010010; A20024; A51076; A51077; A51078; A51081; A51084; B20027; B30076; B30077; B30078; B30081; B30082; B30083; B41005; B51087; B51088; B51089; B51092; B51096; C30087; C30092; C30093; C30094; C30095; C30096; C30097; C30098; C30099; C30102; C41014; C41015; C41017; C41020; C51114; C51118; D20035; D20036; D20037; D20038; D20042; D20043; D20044; D30100; D30101; D30103; D30104; D30105; D30106; D30107; D30108; D30109; E30112; E30113; E30115; E30116; E30117; E30118; E41029; F30120; F30128; F30129; F30131; F30132; F30133; F30134; F30135; G30136; G30137; G30138; G30139; G30140; G30142; H20045; H20047; H20051; H20052; I10010; I41031; I41035; I41036; I41038; I41041; I41042; I41043; I41044; I41045; I41046; I41047; I41048; I41049; I41050; J20055; J20056; J20057; J20059; J20060; J20061; J20063; J20064; K41057; L41066; L41073; A20018; A20023; A30069; A30070; B20026; B20028; B20030; B30084; B30086; C41031; C41018; D20014; I41034; I41037; K41060; L30162; L41068; C51101; C51103; C51111; C51113; D51131; F30122US; F30127; H30149; I41033; I41039; I41040; 010007; E30114; H30144; H30145; H30146; H30147; H30148; H30150; H30151; H30152; H30153; H30155; A30066; A30067; A30071; A51080; A51082; A51085; B41002; B51086; B51090; B51097; C41011; C41061; C41091; C51105; C51108; C51115; C51123; D51127; D51129; D51132; D51135; E41022; E41023; E41024; E41026; F30130; H20048; I41032; K41051; K41052; K41053; K41054; K41059; L41069; A51079; B41004; B41009; A30072; A30073; A30074; A30075; D20039; D20040; E30119; H30154; 010012; A20020; A20034; K41055; K41056; K41058; L30156; L30157; L30159; L30160; L30161; L41067; L41070; L41074; A30068; B51091; B51093; B51094; B51095; C30088; C30089; C30090; C30091; D10005; E41021; E41027; E41028; E41030; L30163; L30167; B51098; C51112; B20032; D51126; D51130; D51133; D51134; L30164; L30166; F30121; F30123; A20015; A20016; A20022; B10001; B20029; B20031; B20033; B30079; B30080; B41001; B41003; B41006; B41007; B41008; B41010; C51102; C51107; C51109; C51110; F30124; F30125; F30126; G30141; H20046; H20049; H20050; H20053; H20054; I10008; I10013; J20058; J20062; L30158; L40161; A20021; L41072. Serial Numbers starting with AF0: 1040-L5; 1045-A6; 1043-L5; 1029-K5; 1037-L5; 1005-I5; 1032-K5; 1036-L5; 1035-L5; 1034-L5; 1033-L5; 1032-L5; 1031-K5; 1030-K5; 1028-K5; 1027-K5; 1026-K5; 1025-K5; 1024-K5; 1023-K5; 1022-K5; 1021-K5; 1020-K5; 1019-K5; 1018-K5; 1017-K5; 1016-K5; 1015-K5; 1014-J5; 1013-J5; 1012-J5; 1011-J5; 1009-I5; 1008-I5; 1007-I5; 1004-I5; 1003-I5; 1001-I5; 1055-A6; 1051-A6; 1048-A6; 1046-A6; 1042-L5; 1010-I5; 1044-A6; 1041-L5; 1038-L5; 1006-I5; 1053-A6; 1052-A6; 1049-A6; 1047-A6; 1039-L5.
Datascope Corp is recalling Anestar and Anestar Plus Anesthesia System. due to The Anestar and Anestar Plus Anesthesia System may produce periods of high Positive End-Expiratory Pressure (PEEP), in both manual and mechanical vent. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The Anestar and Anestar Plus Anesthesia System may produce periods of high Positive End-Expiratory Pressure (PEEP), in both manual and mechanical ventilation mode due to an issue with the Applied Pressure Limit (APL) valve.
Recommended Action
Per FDA guidance
Field correction communications were sent 3/17/2006 to all accounts via certified mail, return receipt requested, signature required.
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