Reported Jul 29, 2020 · Terminated
IntelliVue MX800 patient monitor, model no. 865240
Philips North America, LLC
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: Philips North America, LLC · 3000 Minuteman Rd · Andover, MA · 01810-1032
Is this the product you have?
IntelliVue MX800 patient monitormodel no. 865240
- Lot codes and dates
- Serial numbers
DE50887321DE50887434DE50887128DE50887025DE50887196DE50887429DE50887125DE50887043DE50887303DE50887420DE50887106DE50887164DE50887322DE50887607DE50887061DE50887179DE50887425DE50887427DE50887142DE50887446DE50887152DE50887064DE50887445DE50887137DE50887063
- Serial numbers
- Amount recalled
- 28
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
Some Intellivue MX700/MX800 Patient Monitors were delivered with defective power supplies. The defective power supplies might energize the metal parts of monitor if the grounding instructions were not followed, and may also cause the monitor to stop operating or prevent it from being switched on.
This product could cause temporary or reversible health problems — stop using it.
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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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