Reported Mar 16, 2016 · Terminated
BD Intelliport Medication Management System Sensor The system is indicated for use by healthcare professionals in a…
Becton Dickinson & Company
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: Becton Dickinson & Company · 1 Becton Dr · Franklin Lakes, NJ · 07417-1815
Is this the product you have?
- BD Intelliport Medication Management System Sensor The system is indicated for use by healthcare professionals in a hospital or medical center setting with patients who are receiving manually administered bolus intravenous injections as part of their care to facilitate documentation of the medications.
- Lot codes and dates
Catalog (Ref) # 516700 Lot numbers 52227235251583 and 5253723
- Amount recalled
- 250 units
Where it was sold
Why it was recalled
The sterility of the product cannot be assured. This may result in increased risk of infection.
This product could cause temporary or reversible health problems — stop using it.
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