0 — Class II medical device recall Z-1709-2015
Terminated recall by MRP, LLC dba AMUSA, reported 2015-06-10, distributed in AL, CT, IL, OH, PA, TN. Incorrect expiration date on label
| Recall number | Z-1709-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | MRP, LLC dba AMUSA, Nashville, TN, United States |
| Recall initiated | 2015-04-27 |
| Classified | 2015-06-04 |
| Reported by FDA | 2015-06-10 |
| Terminated | 2016-05-02 |
| Distributed | AL, CT, IL, OH, PA, TN |
| Quantity | 200,000 units |
| Reason classes | labeling |
Product
0.9% Sodium Chloride Injection, USP, Flush Syringe, 10 mL in 12 mL, Sterile, Rx only, Code No. 2T0806 Usage: Flush syringe.
Reason for recall
Incorrect expiration date on label
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-1709-2015. 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.