BD Intelliport Medication Management System Sensor The system is… — Class II medical device recall Z-1076-2016
Terminated recall by Becton Dickinson & Company, reported 2016-03-16, distributed in CA, UT. The sterility of the product cannot be assured. This may result in increased risk of infection.
| Recall number | Z-1076-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Company, Franklin Lakes, NJ, United States |
| Recall initiated | 2015-12-09 |
| Classified | 2016-03-08 |
| Reported by FDA | 2016-03-16 |
| Terminated | 2017-01-09 |
| Distributed | CA, UT |
| Quantity | 250 units |
| Reason classes | sterility |
| Lot numbers | 5222723, 5251583, 5253723 |
| Model numbers | 516700, 5222723, 5251583, 5253723 |
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 for recall
The sterility of the product cannot be assured. This may result in increased risk of infection.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1076-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.