Reported Feb 14, 2024 · Ongoing
Flow-e Anesthesia System, model 6887900
Getinge USA Sales Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.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: Getinge Usa Sales Inc · 1 Geoffrey Way · Wayne, NJ · 07470-2035
Is this the product you have?
- Flow-e Anesthesia System, model 6887900
- Lot codes and dates
- UDI-DI07325710010457
- serial numbers (US)
86 of 86 codes
500125003050031500335003450035500365003750038500395004050041500425004350046500475004850051500525005350054500555005650057500585005950060500695007050071500725007350074500845008550086500875008850089500905009150092500935009450096500975010850109501105011150132501545015550193501945019550196501975019950211
- Amount recalled
- 86 (US)
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation.
This product could cause temporary or reversible health problems — stop using it.
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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