FDA Device recall Z-0465-2025
Medline Iris Scissors, Single-Use, Curved, Standard 4.5 , Model Nos
- FDA Device
- Class II
- ongoing
- Published 2024-11-20
On 2024-11-20 the FDA classified a Class II recall of Medline Iris Scissors, Single-Use, Curved, Standard 4.5 , Model Nos by Medline Industries Northfield, citing tip protector may fall off within the packaging, resulting in compromised sterile barrier system and loss of sterility.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0465-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-10-21 |
| Published | 2024-11-20 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
Medline Iris Scissors, Single-Use, Curved, Standard 4.5 , Model Nos. DYNJ04049 (cases), DYNJ04049H (eaches)
Reason
Tip protector may fall off within the packaging, resulting in compromised sterile barrier system and loss of sterility.
Identifiers
| code_info | UDI-DI: 10080196847273 Lots 23GBV681 23HBD138 23IBF254 23LBJ787 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0465-2025%22
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