FDA Device recall Z-1703-2016
WHIN Infusion Set - 90 Huber Needle and Wing (22 ga/1in)
- FDA Device
- Class II
- terminated
- Published 2016-06-01
On 2016-06-01 the FDA classified a Class II recall of WHIN Infusion Set - 90 Huber Needle and Wing (22 ga/1in) by B Braun Medical, citing potential for the tip of the Huber needle on the WHIN Infusion Set to protrude from the needle guard.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1703-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-04-26 |
| Published | 2016-06-01 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | B Braun Medical |
| Distribution | AL, AR, CA, FL, GA, IL, IN, KY, MA, MS, NJ, NV, OH, PA, SC, TN, TX, VA |
Product
WHIN Infusion Set - 90 Huber Needle and Wing (22 ga/1in). Intravenous delivery through intravascular ports, 20 units per case, Catalog Number 471734. Usage: Infusion of solution/medication into implanted intravascular ports.
Reason
Potential for the tip of the Huber needle on the WHIN Infusion Set to protrude from the needle guard.
Identifiers
| code_info | Catalog Number 471734, Lot Numbers: 0061482060 and 0061486821, expiration dates :1/31/2021 and 02/28/2021, respectively. |
|---|
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-1703-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.