Reported May 6, 2015 · Terminated
Introduction Pack. A device inserted into an endotracheal tube to aid in the intubation procedure.
Vital Signs Colorado 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: Vital Signs Colorado Inc. · 11039 East Lansing Circle · Englewood, CO · 80112-5909
Is this the product you have?
- Introduction Pack. A device inserted into an endotracheal tube to aid in the intubation procedure.
- Lot codes and dates
- Catalog Number 3960
- Amount recalled
- 399
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand Stylet catalog numbers 3910 and 3960 due to a potential patient safety risk involving a breach in the sterile packaging that may not be recognized prior to use.
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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