CLASS I ONGOING Device recall · Reported 20 Nov 2024 · FDA Enforcement Report
Atlan A350 recalled by Draeger Medical
Draeger Medical is recalling Atlan A350, distributed nationwide in the US. The recall was initiated on 15 Oct 2024 and the FDA has classified it as Class I.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0304-2025
- FDA event ID
- 95561
- Recalling firm
- Draeger Medical, Telford, PA
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 15 Oct 2024
- FDA classified
- 13 Nov 2024
- Reported
- 20 Nov 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Device Malfunction
- Device type
- Medical Software
Timeline
| 15 Oct 2024 | Recall initiated by company | |
| 13 Nov 2024 | Classified by FDA | +29 days |
| 20 Nov 2024 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.
Product as listed by the FDA
Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Component: Not applicable
Where it was distributed
US Nationwide distribution in the states of AL, AZ, CA, FL, GA, IA, IL, KY, MA, ME, ND, NE, NH, NJ, NY, OH, PA, TN, TX, WI, WY. International distribution: Argentina, Australia, Austria, Azerbaijan, Bahrain, Belgium, Brazil, Bulgaria, Cambodia, Canada, Chili, China, Columbia, Croatia, Czech Republic, Egypt, El Salvador, Estonia, Finland, France, Germany, Greece, Hungary, India, Indonesia, Ireland, Italy, Japan, Jordan, Kazakhstan, Kenya, Latvia, Malaysia, Mauritius, Mexico, Morocco, Namibia, Nepal, Pakistan, Panama, Peru, Philippines, Poland, Portugal, Reunion, Romania, Russian Federation, Saudi Arabia, Serbia, Slovakia, Slovenia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, Ukraine, United Kingdom, Uruguay, United Arab Emirates, Vietnam.
Nationwide AlabamaArizonaCaliforniaFloridaGeorgiaIowaIllinoisKentuckyMassachusettsMaineNorth DakotaNebraskaNew HampshireNew JerseyNew YorkOhioPennsylvaniaTennesseeTexasWisconsin
Questions about this recall
Is Atlan A350 recalled?
Yes. Draeger Medical recalled Atlan A350 on 15 Oct 2024. The recall is Class I and its status is Ongoing. Recall number Z-0304-2025.
Why was it recalled?
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
Which lots are affected?
Model/Catalog Number: 8211500; UDI-DI Number: 04048675556176; Serial Numbers Distributed in the US: ASTB-0038; 0039; 0146; 0147; 0148; 0281; 0282; 0283; 0300; 0301; 0302; 0303; 0312; 0313; 0314; 0315; 0316 ASTC-0005; 0094; 0095; 0190; 0191 ASTD-0029; 0030; 0031; 0032; 0033; 0034; 0035; 0036; 0037; 0038; 0039; 0040; 0041; 0042; 0043; 0044; 0045; 0046 0057; 0136; 0137; 0138; 0139; 0140; 0141; 0142; 0143; 0148; 0149; 0150; 0151; 0152; 0153; 0155; 0156; 0157; 0158; 0170; 0171; 0186; 0235; 0236; 0237; 0257; 0258; 0259 ASTE-0002; 0003; 0004; 0005; 0006; 0007; 0008; 0029; 0030; 0031; 0032; 0080; 0134; 0135; 0136; 0152; 0153; 0154; 0155; 0180; 0181; 0209; 0210; 0211; 0212; 0213; 0214; 0215; 0216; 0217; 0218; 0254; 0255; 0318; 0319; 0320; 0321; 0322 ASTF-0007; 0008; 0009; 0010; 0145; 0146; 0147; 0148; 0149; 0150; 0177; 0178; 0379; 0380 ASTH-0083; 0084; 0107; 0160; 0161; 0184; 0185; 0207; 0208; 0233; 0241; 0242; 0254; 0370; 0392; 0432; 0464 Serial Numbers Distributed OUS ASTA-0279; 0293; 0302; 0303; 0304; 0306; 0334; 0335; 0336; 0344; 0347; 0348; 0360; 0369; 0373; 0375; 0376; 0377; 0379; 0380; 0381; 0386; 0389; 0390; 0392; 0393; 0399; 0412; 0422; 0433; 0435; 0437; 0438 ASTB-0009; 0011; 0012; 0015; 0016; 0017; 0019; 0024; 0025; 0026; 0027; 0035; 0036; 0042; 0043; 0044; 0045; 0047; 0050; 0056; 0058; 0059; 0060; 0062; 0067; 0069; 0070; 0072; 0073; 0085; 0086; 0087; 0088; 0089; 0090; 0091; 0092; 0096; 0097; 0098; 0099; 0100; 0101; 0102; 0104; 0105; 0106; 0107; 0108; 0109; 0110; 0111; 0112; 0113; 0114; 0115; 0116; 0117; 0118; 0119; 0120; 0121; 0123; 0124; 0125; 0126; 0127; 0128; 0129; 0130; 0131; 0132; 0133; 0135; 0136; 0137; 0138; 0139; 0140; 0141; 0142; 0143; 0144; 0145; 0147; 0149; 0152; 0153; 0154; 0155; 0156; 0157; 0158; 0159; 0163; 0164; 0166; 0167; 0168; 0169; 0170; 0171; 0172; 0173; 0174; 0183; 0184; 0185; 0186; 0187; 0188; 0189; 0190; 0191; 0192; 0193; 0194; 0196; 0197; 0198; 0199; 0200; 0201; 0202; 0203; 0204; 0205; 0207; 0208; 0209; 0210; 0212; 0213; 0221; 0222; 0223; 0224; 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0282; 0283; 0284 ASTE-0009; 0010; 0011; 0018; 0019; 0020; 0021; 0022; 0023; 0024; 0025; 0026; 0027; 0028; 0033; 0036; 0037; 0038; 0039; 0040; 0045; 0046; 0047; 0048; 0049; 0050; 0051; 0052; 0053; 0054; 0055; 0061; 0066; 0067; 0068; 0069; 0070; 0071; 0072; 0073; 0074; 0075; 0076; 0081; 0082; 0088; 0089; 0090; 0091; 0092; 0093; 0094; 0095; 0096; 0097; 0098; 0099; 0100; 0101; 0102; 0103; 0104; 0105; 0106; 0107; 0109; 0110; 0111; 0112; 0113; 0114; 0115; 0116; 0117; 0118; 0119; 0120; 0121; 0132; 0133; 0137; 0138; 0139; 0140; 0141; 0142; 0143; 0144; 0145; 0146; 0147; 0148; 0149; 0150; 0151; 0156; 0157; 0158; 0159; 0160; 0161; 0162; 0167; 0168; 0169; 0170; 0182; 0183; 0184; 0185; 0186; 0188; 0189; 0190; 0191; 0192; 0193; 0194; 0204; 0205; 0206; 0207; 0208; 0227; 0228; 0229; 0230; 0231; 0232; 0233; 0234; 0235; 0236; 0237; 0238; 0239; 0240; 0241; 0242; 0251; 0252; 0253; 0256; 0257; 0258; 0259; 0260; 0261; 0262; 0263; 0264; 0265; 0266; 0267; 0268; 0269; 0270; 0271; 0272; 0273; 0274; 0275; 0276; 0277; 0283; 0284; 0285; 0286; 0287; 0288; 0289; 0290; 0291; 0292; 0293; 0294; 0295; 0296; 0297; 0298; 0307; 0308; 0309; 0310; 0311; 0312; 0313; 0314; 0315; 0316; 0317; 0323; 0324; 0330; 0331; 0332; 0333; 0334; 0335; 0336; 0337; 0338; 0339; 0340; 0341; 0342; 0343; 0344; 0345; 0346; 0347; 0363; 0364; 0365; 0366; 0367; 0368; 0369; 0376 ASTF-0011; 0012; 0013; 0020; 0021; 0022; 0023; 0024; 0025; 0026; 0038; 0039; 0040; 0041; 0042; 0043; 0044; 0045; 0046; 0047; 0056; 0057; 0058; 0059; 0060; 0064; 0065; 0066; 0067; 0068; 0069; 0083; 0084; 0085; 0087; 0088; 0089; 0090; 0091; 0092; 0094; 0095; 0096; 0097; 0098; 0099; 0100; 0101; 0102; 0103; 0104; 0105; 0106; 0107; 0108; 0109; 0114; 0115; 0116; 0117; 0120; 0126; 0127; 0128; 0129; 0130; 0131; 0132; 0133; 0134; 0142; 0143; 0144; 0152; 0153; 0154; 0156; 0157; 0158; 0159; 0160; 0161; 0163; 0164; 0165; 0171; 0172; 0173; 0174; 0175; 0176; 0179; 0180; 0181; 0182; 0183; 0184; 0185; 0186; 0187; 0188; 0189; 0190; 0191; 0192; 0193; 0199; 0200; 0201; 0202; 0203; 0204; 0205; 0206; 0207; 0208; 0209; 0210; 0211; 0212; 0213; 0214; 0215; 0216; 0217; 0218; 0219; 0223; 0224; 0225; 0226; 0227; 0228; 0229; 0230; 0231; 0232; 0233; 0234; 0235; 0236; 0237; 0238; 0239; 0240; 0241; 0242; 0243; 0244; 0245; 0246; 0247; 0248; 0249; 0250; 0251; 0252; 0253; 0254; 0255; 0256; 0257; 0258; 0259; 0260; 0261; 0262; 0263; 0264; 0265; 0266; 0267; 0268; 0269; 0270; 0271; 0272; 0273; 0274; 0275; 0276; 0277; 0278; 0279; 0280; 0281; 0282; 0283; 0284; 0285; 0286; 0287; 0288; 0289; 0290; 0291; 0292; 0293; 0294; 0295; 0296; 0297; 0298; 0299; 0300; 0302; 0303; 0304; 0305; 0306; 0307; 0308; 0309; 0310; 0311; 0312; 0313; 0314; 0315; 0316; 0317; 0318; 0319; 0320; 0321; 0322; 0323; 0324; 0325; 0326; 0327; 0328; 0329; 0330; 0331; 0332; 0333; 0334; 0335; 0336; 0337; 0338; 0339; 0340; 0341; 0342; 0343; 0344; 0345; 0346; 0347; 0348; 0349; 0350; 0351; 0352; 0353; 0354; 0355; 0356; 0357; 0358; 0359; 0360; 0361; 0362; 0363; 0364; 0365; 0366; 0367; 0368; 0369; 0370; 0371; 0372; 0373; 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Where was it sold?
US Nationwide distribution in the states of AL, AZ, CA, FL, GA, IA, IL, KY, MA, ME, ND, NE, NH, NJ, NY, OH, PA, TN, TX, WI, WY. International distribution: Argentina, Australia, Austria, Azerbaijan, Bahrain, Belgium, Brazil, Bulgaria, Cambodia, Canada, Chili, China, Columbia, Croatia, Czech Republic, Egypt, El Salvador, Estonia, Finland, France, Germany, Greece, Hungary, India, Indonesia, Ireland, Italy, Japan, Jordan, Kazakhstan, Kenya, Latvia, Malaysia, Mauritius, Mexico, Morocco, Namibia, Nepal, Pakistan, Panama, Peru, Philippines, Poland, Portugal, Reunion, Romania, Russian Federation, Saudi Arabia, Serbia, Slovakia, Slovenia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, Ukraine, United Kingdom, Uruguay, United Arab Emirates, Vietnam.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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