BD Intelliport Medication Management System Sensor The recall: Sterility Concern
BD Intelliport Medication Management System Sensor The system is indicated for use by healthcare professionals in a hospital or medical center setting…
Why was BD Intelliport Medication Management System Sensor The recalled?
The sterility of the product cannot be assured. This may result in increased risk of infection.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Catalog (Ref) # 516700 Lot numbers 5222723, 5251583 and 5253723.
- Product
- BD Intelliport Medication Management System Sensor The system is indicated for use by healthcare professionals in a hospital or medical center setting…
- Recalling firm
- Becton Dickinson & Company
- Quantity
- 250 units
- Distribution
- US Distribution to:California and Utah.
- Recall date
- March 16, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)