Reported Oct 30, 2024 · Ongoing
Welch Allyn Life2000 Ventilation System, REF MS-01-0118, within exterior carton codes: 1) BT-20-0002, 2) BT-20-0002A,…
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?
Welch Allyn Life2000 Ventilation SystemREF MS-01-0118
- within exterior carton codes
1) BT-20-00022) BT-20-0002A3) BT-20-0002AP4) BT-20-00075) BT-20-0011and 6) RMS010118CP
- Lot codes and dates
- UDI/DI 00887761978089 or 00815410020537, All Life2000 Ventilators with software version 06.08.00.00
- Amount recalled
- 10,957 units
This recall covers 10 products
The agency filed one notice per product. You are reading one of them; the other 9 are below.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
The Life2000 ventilator may fail to initiate the Low Gas Pressure alarm if the pressure gas source (Life2000 compressor, oxygen cylinder or wall source) is not supplied to the ventilator before initiating therapy.
Using this product could cause serious injury, illness or death — stop using it now.
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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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