Terumo Needle — Class II medical device recall Z-2005-2019
Terminated recall by Terumo Medical Corporation, reported 2019-07-31, distributed in FL, IN, KS, KY, MA, MO, NH, NV…. There is a potential for a loss of package integrity that may compromise the sterility of the product.
| Recall number | Z-2005-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Terumo Medical Corporation, Elkton, MD, United States |
| Recall initiated | 2019-02-08 |
| Classified | 2019-07-22 |
| Reported by FDA | 2019-07-31 |
| Terminated | 2020-05-08 |
| Distributed | FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, TX |
| Quantity | 30,000 |
| Reason classes | sterility, packaging |
| Lot numbers | 180811C |
Product
Terumo Needle, 23G x 1", Product Code NN2325R
Reason for recall
There is a potential for a loss of package integrity that may compromise the sterility of the product.
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-2005-2019. 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.