FDA Device recall Z-2358-2019
Medline SYRINGE, PISTON,IRR TRAY,W/.9, REF DYNC2303
- FDA Device
- Class II
- ongoing
- Published 2019-09-04
On 2019-09-04 the FDA classified a Class II recall of Medline SYRINGE, PISTON,IRR TRAY,W/.9, REF DYNC2303 by Medline Industries, citing samples in the identified lot were found to have incomplete or open packaging seals.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2358-2019 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2019-08-09 |
| Published | 2019-09-04 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Medline Industries |
| Distribution | US |
Product
Medline SYRINGE, PISTON,IRR TRAY,W/.9, REF DYNC2303. Sterile Piston Irrigation Syringe Tray with Saline
Reason
Samples in the identified lot were found to have incomplete or open packaging seals.
Identifiers
| code_info | Lot Number 19CAB954 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2358-2019%22
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