Draeger Medical, Inc. Medical Air Compressor Model #8413419 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medical Air Compressor Model #8413419
Brand
Draeger Medical, Inc.
Lot Codes / Batch Numbers
Model number 8413419. Catalog number 8413419. Serial Numbers ARXC-001, ARXC-0002, ARXC-0009, ARXC-0011, ARXC-0012, ARXC-0013, ARXC-0014, ARXC-0015, ARXC-0016, ARXC-0017, ARXC-0019, ARXC-0020, ARXD-0034, ARXD-0035, ARXD-0036, ARXD-0037, ARXD-0038, ARXD-0039, ARXD-0040, ARXE-0081, ARXE-0082, ARXE-0083, ARXE-0084, ARXE-0085, ARXE-0086, ARXE-0087, ARXE-0088, ARXE-0089, ARXE-0090, ARXE-0091, ARXE-0092, ARXE-0093, ARXE-0094, ARXE-0095, ARXE-0096, ARXE-0097, ARXE-0098, ARXE-0099, ARXE0100, ARXE-0101, ARXE-0102, ARXE-0103, ARXE-0104, ARXE-0106, ARXE-0107, ARXE-0108, ARXE-0109, ARXE-0110, ARXE-0111, ARXE-0112, ARXE-0113, ARXE-0114, ARXE-0115, ARXE-0116, ARXE-0117, ARXE-0118, ARXE-0119, ARXE-0120, ARXE-0121, ARXE-0122, ARXE-0123, ARXE-0124, ARXE-0125, ARXE-0126, ARXE-0127, ARXE-0128, and ARXE-0129.
Products Sold
Model number 8413419. Catalog number 8413419. Serial Numbers ARXC-001; ARXC-0002; ARXC-0009; ARXC-0011; ARXC-0012; ARXC-0013; ARXC-0014; ARXC-0015; ARXC-0016; ARXC-0017; ARXC-0019; ARXC-0020; ARXD-0034; ARXD-0035; ARXD-0036; ARXD-0037; ARXD-0038; ARXD-0039; ARXD-0040; ARXE-0081; ARXE-0082; ARXE-0083; ARXE-0084; ARXE-0085; ARXE-0086; ARXE-0087; ARXE-0088; ARXE-0089; ARXE-0090; ARXE-0091; ARXE-0092; ARXE-0093; ARXE-0094; ARXE-0095; ARXE-0096; ARXE-0097; ARXE-0098; ARXE-0099; ARXE0100; ARXE-0101; ARXE-0102; ARXE-0103; ARXE-0104; ARXE-0106; ARXE-0107; ARXE-0108; ARXE-0109; ARXE-0110; ARXE-0111; ARXE-0112; ARXE-0113; ARXE-0114; ARXE-0115; ARXE-0116; ARXE-0117; ARXE-0118; ARXE-0119; ARXE-0120; ARXE-0121; ARXE-0122; ARXE-0123; ARXE-0124; ARXE-0125; ARXE-0126; ARXE-0127; ARXE-0128; and ARXE-0129.
Draeger Medical, Inc. is recalling Medical Air Compressor Model #8413419 due to Compressors not providing sufficient supply pressure to connected medical ventilator. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Compressors not providing sufficient supply pressure to connected medical ventilator
Recommended Action
Per FDA guidance
The recalling firm issued a Medical Device Recall Letter dated 1/22/07 to their customers via Certified Mail. An authorized service representative will inspect each potentially affected device. If a device is found to have an affected dryer assembly, it will be repaired free of charge.
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