Class I Recall

Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Component:

Summary

The FDA issued a Class I for Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Soft 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-0304-2025

Action Date

2024-11-20

Status

Ongoing

Product Description

Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Component: Not applicable

Lot/Code Info: 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; 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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; 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Quantity Affected: 1,492 units (139 units US, 1,353 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

Draeger Medical, Inc.

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-0304-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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