Life2000 Ventilator recall
Life2000 Ventilator , REF MS-01-0118, ventilatory support for the care of individuals
Why was Life2000 Ventilator recalled?
There is the potential for patient desaturation events to occur under certain scenarios when the Life2000 ventilation system is connected with an oxygen concentrator.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI 00887761978089, Serial Numbers: L1912010-050, L1905010-081, L1912010-037, L1903102-024, L1912025-024, L1903103-011, L1911019-026, L1912013-045, L1912013-036, L1905010-028, L1903102-028, L1905010-089, L1912013-019, L1903102-010, L1903103-026, L1905010-058, L1903097-007, L1903103-003, L1905010-092, L1903102-019, L1903102-013, L1904038-002, L1905010-051, L1903097-012, L1905010-018, L1904038-001, L1903103-004, L1912013-032, L1904038-003, L1911019-025, L1904050-001, L1905010-059, L1905010-088, L1911019-033, L1903103-001, L1903103-009, L1912013-013, L1903102-025, L1903103-002, L1912013-006, L1911019-010, L1912010-030, L1903097-018, L1912025-021, L1905010-004, L1903103-030, L1911019-027, L1903102-020, L1905010-041, L1912013-031, L1905010-033, L1905010-056, L1912013-041, L1905010-082, L1912010-003, L1912010-035, L1903103-014, L1912013-035, L1912010-034, L1912013-008, L1903103-027, L1903103-007, L1911019-014, L1905010-021, L1912025-019, L1903103-012, L1911019-037, L1912010-002, L1903103-010, L2001042-022, L1912025-007
- Product
- Life2000 Ventilator , REF MS-01-0118, ventilatory support for the care of individuals
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 71 units
- Distribution
- Nationwide
- Recall date
- March 8, 2023
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)