FDA Device recall Z-2089-2019
Acuject Variable Injection Needle
- FDA Device
- Class II
- terminated
- Published 2019-08-07
On 2019-08-07 the FDA classified a Class II recall of Acuject Variable Injection Needle by Wilson Cook Medical, citing potential for occluded injection needles.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2089-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-06-14 |
| Published | 2019-08-07 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Wilson Cook Medical |
| Distribution | n/a |
Product
Acuject Variable Injection Needle
Reason
Potential for occluded injection needles.
Identifiers
| code_info | Lot Code W413079; Catalog Number VIN-25; Expiration Date 10/24/2021; UDI Number (01)00827002225268(17)211024(10)W4136079 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
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All Wilson Cook Medical recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2089-2019%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.