Reported May 21, 2025 · Ongoing
Welch Allyn Life2000 Ventilation system, Product Codes
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 system, Product Codes
8 of 8 products
| Model / number | Product as published |
|---|---|
BT-20-0002 | Welch Allyn Life2000 Ventilation system, Product Codes: 1) |
BT-20-0002A | 2) |
BT-20-0002AP | 3) |
BT200007 | 4) |
BT-20-0007 | 5) |
BT200011 | 6) |
BT-20-0011 | 7) |
RMS010118CP. | 8) |
- Lot codes and dates
8 of 8 products
Products covered by this recall # Barcodes Product as published 1 0081541002053700887761978089BT-20-0002, UDI/DI 00815410020537 or 00887761978089 2 0081541002053700887761978089BT-20-0002A, UDI/DI 00815410020537 of 00887761978089 3 0081541002053700887761978089BT-20-0002AP, UDI/DI 00815410020537 or 00887761978089 4 0081541002027800887761978089BT200007, UDI/DI 00815410020278 or 00887761978089 5 0081541002027800887761978089BT-20-0007, UDI/DI 00815410020278 or 00887761978089 6 0081541002053700887761978089BT200011, UDI/DI 00815410020537 or 00887761978089 7 0081541002053700887761978089BT-20-0011, UDI/DI 00815410020537 or 00887761978089 8 0081541002053700887761978089RMS010118CP, UDI/DI 00815410020537 or 00887761978089. - Amount recalled
- 4881 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Why it was recalled
Stop using this product now
A cybersecurity vulnerability was discovered through internal testing.
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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