FDA Device recall Z-1210-2019
SmartSite Syringe Administration Set-Product Package Size 50, Catalog Number: 10798696
- FDA Device
- Class I
- terminated
- Published 2019-07-03
On 2019-07-03 the FDA classified a Class I recall of SmartSite Syringe Administration Set-Product Package Size 50, Catalog Number: 10798696 by Becton Dickinson And, citing leaking of the Smartsite Syringe Administration Set. May result in delay or interruption of infusion, under-infusion, contamination of the fluid path and HCP exposure to infusates.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1210-2019 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2019-02-28 |
| Published | 2019-07-03 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Becton Dickinson And |
| Distribution | US |
Product
SmartSite Syringe Administration Set-Product Package Size 50, Catalog Number: 10798696
Reason
Leaking of the Smartsite Syringe Administration Set. May result in delay or interruption of infusion, under-infusion, contamination of the fluid path and HCP exposure to infusates.
Identifiers
| code_info | Lot Number: 18046218 Exp. Date: 04/18/2021 UDI: 50885403234352 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1210-2019%22
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