FDA Device recall Z-0921-2026
SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
- FDA Device
- Class II
- ongoing
- Published 2025-12-24
On 2025-12-24 the FDA classified a Class II recall of SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000 by Medline Industries, citing the items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0921-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-11-13 |
| Published | 2025-12-24 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries |
| Distribution | US |
Product
SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
Reason
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
Identifiers
| code_info | DYND04000, UDI-DI: 10193489191349(each), 20193489191346(case), Lot Number: 2023102590 |
|---|
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-0921-2026%22
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