FDA Device recall Z-1709-2015
0.9% Sodium Chloride Injection, USP, Flush Syringe, 10 mL in 12 mL, Sterile, Rx only, Code No. 2T0806 Usage: Flush syringe
- FDA Device
- Class II
- terminated
- Published 2015-06-10
On 2015-06-10 the FDA classified a Class II recall of 0.9% Sodium Chloride Injection, USP, Flush Syringe, 10 mL in 12 mL, Sterile, Rx only, Code No. 2T0806 Usage: Flush syringe by Mrp, citing incorrect expiration date on label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1709-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-04-27 |
| Published | 2015-06-10 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Mrp |
| Distribution | AL, CT, IL, OH, PA, TN |
Product
0.9% Sodium Chloride Injection, USP, Flush Syringe, 10 mL in 12 mL, Sterile, Rx only, Code No. 2T0806 Usage: Flush syringe.
Reason
Incorrect expiration date on label
Identifiers
| code_info | CODES: KH04103, KH04104, KH04105 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1709-2015%22
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