FDA Device recall Z-2006-2019
Terumo Needle, 30G x 1/2", Product Code NN3013R
- FDA Device
- Class II
- terminated
- Published 2019-07-31
On 2019-07-31 the FDA classified a Class II recall of Terumo Needle, 30G x 1/2", Product Code NN3013R by Terumo Medical, citing there is a potential for a loss of package integrity that may compromise the sterility of the product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2006-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-02-08 |
| Published | 2019-07-31 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Terumo Medical |
| Distribution | FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, TX |
Product
Terumo Needle, 30G x 1/2", Product Code NN3013R
Reason
There is a potential for a loss of package integrity that may compromise the sterility of the product.
Identifiers
| code_info | Lot Numbers 181005C |
|---|
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-2006-2019%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.