Reported Mar 8, 2023 · Ongoing

Life2000 Ventilator System, a) REF BT-20-0002, b) REF BT-20-0002A, ventilatory support for the care of individuals

Baxter Healthcare Corporation

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625

Is this the product you have?

  • Life2000 Ventilator System, a) REF BT-20-0002, b) REF BT-20-0002A, ventilatory support for the care of individuals
Lot codes and dates
    • a) REF BT-20-0002
    • UDI 00887761978089
  • Serial Numbers

    2,325 of 2,325 codes

    • 120370002037
    • 120370001516
    • 120370001522
    • L2005055-910
    • 120300000056
    • 120370002035
    • 120370001529
    • 120370001518
    • 120370001514
    • 120370001909
    • 120370001971
    • 120360000581
    • 120370001980
    • 120370002002
    • 120380000643
    • 120370001975
    • 120370002042
    • 120370002030
    • 120370002105
    • 120370000385
    • 120380000419
    • L1903097-020
    • L2002011-022
    • L2002011-007
    • L2001042-044
    • 120370002039
    • 120380000532
    • 120370002025
    • 120370001961
    • 120370002107
    • 120370000386
    • 120370002027
    • 120370002034
    • 120350000951
    • 120370001519
    • 120370002036
    • 120370002001
    • 120370002092
    • 120380000420
    • 120370001523
    • 120380000636
    • 120380000644
    • 120370002031
    • 120340000517
    • 120350000961
    • 120330000935
    • 120310001578
    • 120330000936
    • 120370001513
    • L1912025-010
    • L191025-031
    • L1904050-005
    • L1911019-032
    • L1904050-015
    • L1912025-041
    • L1904050-010
    • L1904038-012
    • L1904050-007
    • L1912025-005
    • L1912025-033
Amount recalled
4279 units

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

There is the potential for patient desaturation events to occur under certain scenarios when the Life2000 ventilation system is connected with an oxygen concentrator.

Using this product could cause serious injury, illness or death — stop using it now.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:20 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.