Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Componen
Summary
The FDA issued a Class I for Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 So by Draeger Medical, Inc.. Reason: The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation du.
Details
Source
Device Recall
External ID
Z-0305-2025
Action Date
2024-11-20
Status
Ongoing
Category
device
Product Description
Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Component: Not applicable
Lot/Code Info: Model/Catalog Number: 8621600; UDI-DI Number: 04048675556183; Serial Numbers Distributed in the US: ASTA-0307; 0309; 0311; 0349; 0350; 0351; 0353; 0363; 0365; 0394; 0408; 0409 ASTB-0048; 0286; 0287; 0288; 0289; 0290; 0291; 0304; 0305; 0306; 0307; 0308; 0309; 0317; 0318; 0319; 0320; 0321; 0322 ASTC-0006; 0007; 0068; 0069; 0070; 0082; 0083; 0099; 0100; 0101; 0105; 0106; 0107; 0108; 0109; 0118; 0119; 0136; 0137; 0229; 0230; 0243; 0244; 0245 ASTD-0008; 0009; 0010; 0011; 0012; 0013; 0014; 0129; 0130; 0131; 0132; 0133; 0134; 0135; 0154; 0159; 0160; 0161; 0162; 0163; 0164; 0165; 0166; 0167; 0168; 0169; 0181; 0182; 0183; 0193; 0194; 0195; 0225; 0226; 0227; 0228; 0229; 0230; 0231; 0238; 0239; 0240; 0241; 0242; 0243; 0244; 0245 ASTE-0016; 0017; 0077; 0078; 0079; 0086; 0087; 0122; 0123; 0124; 0125; 0126; 0129; 0130; 0131; 0163; 0164; 0165; 0166; 0171; 0172; 0173; 0174; 0195; 0196; 0197; 0198; 0203; 0225; 0226; 0246; 0247; 0248; 0249; 0250; 0278; 0279; 0280; 0281; 0301; 0302; 0303; 0304; 0305; 0306; 0348; 0349; 0350; 0351; 0352; 0357; 0358; 0359; 0360; 0361; 0362 ASTF-0001; 0002; 0003; 0004; 0014; 0015; 0016; 0017; 0018; 0030; 0031; 0032; 0033; 0034; 0035; 0036; 0037; 0055; 0061; 0062; 0063; 0070; 0071; 0076; 0077; 0078; 0079; 0080; 0081; 0121; 0122; 0123; 0124; 0125; 0135; 0136; 0137; 0138; 0139; 0140; 0141; 0168; 0169; 0170; 0194; 0195; 0196; 0409; 0410; 0411; 0436; 0437; 0438; 0474; 0475; 0476; 0477; 0478 ASTH-0007; 0008; 0009; 0010; 0011; 0012; 0092; 0093; 0094; 0095; 0096; 0120; 0121; 0122; 0123; 0124; 0125; 0126; 0142; 0143; 0144; 0145; 0146; 0147; 0148; 0169; 0170; 0171; 0172; 0173; 0174; 0175; 0187; 0188; 0189; 0190; 0191; 0192; 0269; 0270; 0271; 0272; 0273; 0293; 0294; 0295; 0296; 0306; 0307; 0308; 0309; 0310; 0311; 0324; 0325; 0326; 0327; 0330; 0331; 0332; 0333; 0334; 0335; 0336; 0337; 0338; 0339; 0358; 0359; 0360; 0361; 0362; 0363; 0364; 0365; 0383; 0384; 0385; 0386; 0387; 0388; 0389; 0390; 0450; 0476; 0477; 0478; 0479; 0480; 0481; 0488; 0489; 0490; 0491 Serial Numbers Distributed OUS: ASTA-0253; 0289; 0290; 0327; 0362; 0404; 0405; 0426; 0427; 0428; 0429; 0430 ASTB-0003; 0005; 0007; 0028; 0029; 0030; 0031; 0032; 0033; 0075; 0076; 0077; 0079; 0080; 0081; 0082; 0083; 0084; 0134; 0195; 0206; 0219; 0220; 0237 ASTC-0001; 0002; 0003; 0004; 0026; 0138; 0163; 0180; 0181; 0194; ASTD-0015; 0016; 0050; 0061; 0062; 0063; 0064; 0065; 0066; 0203; 0204; 0205; 0265; 0266; 0267 ASTE-0034; 0035; 0057; 0058; 0059; 0060; 0062; 0085; 0108; 0127; 0128; 0175; 0202; 0223; 0224; 0300; 0325; 0326; 0327; 0328; 0329; 0353; 0354; 0355; 0356 ASTF-0051; 0052; 0053; 0054; 0112; 0113; 0435; 0471 ASTH-0039; 0040; 0045; 0046; 0081; 0082; 0176; 0193; 0194; 0204; 0217; 0218; 0219; 0225; 0226; 0243; 0244; 0245; 0246; 0255; 0256; 0382; 0403; 0404; 0405; 0406; 0434; 0435; 0436; 0437; 0451; 0452; 0453; 0 ASTJ-0063; 0064; 0065; 0066; 0067; 0068; 0089; 0090; 0091; 0092; 0145; 0146; 0147; 0171; 0237 ASTK-0002
Quantity Affected: 455 units (310 units US, 145 OUS)
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.
Distribution
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-15
Company
Telford, PA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 242 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Draeger Medical, Inc. has 37 FDA actions in our database, including 37 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Draeger Medical, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Draeger Medical, Inc. have FDA actions?
Draeger Medical, Inc. has 37 FDA actions in our database, including 37 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-0305-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
Want to know the moment something like this happens?
Get alerts for deviceRelated Actions
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, IC Tray REF: 888810200
Covidien LP · 2023-08-23
Sterile Procedural Trays, labeled as the following: a. BREAST AUGMENTATION b. BREAST REDUCTION CDS c. CUH ABDOMINO
MEDLINE INDUSTRIES, LP - Northfield · 2023-02-15
VTC Regular Kit Nephrostomy Catheter System Kit, Material Number REF M001245300; to provide external drainage of the uri
Boston Scientific Corporation · 2024-09-25
EnChroma Safety Glasses with Rx Indoor Universal Lenses: Martinez Cx1 Indoor Rx, SKU: Cx.PC.IN.MTZ.BK.Rx; Summit Indoo
Enchroma Inc · 2024-11-27
Otological Ventilation Tube - T-Tube 9mm - Silicone; Product Code: NZ3309;
Adept Medical Ltd · 2025-01-29