FDA Device recall Z-1076-2016
BD Intelliport Medication Management System Sensor The system is indicated for use by healthcare professionals in a hospital or medical cen…
- FDA Device
- Class II
- terminated
- Published 2016-03-16
On 2016-03-16 the FDA classified a Class II recall of BD Intelliport Medication Management System Sensor The system is indicated for use by healthcare professionals in a hospital or medical cen… by Becton Dickinson And, citing the sterility of the product cannot be assured. This may result in increased risk of infection.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1076-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-12-09 |
| Published | 2016-03-16 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Becton Dickinson And |
| Distribution | CA, UT |
Product
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.
Reason
The sterility of the product cannot be assured. This may result in increased risk of infection.
Identifiers
| code_info | Catalog (Ref) # 516700 Lot numbers 5222723, 5251583 and 5253723. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1076-2016%22
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