FDA Device recall Z-2275-2026
PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
- FDA Device
- Class II
- ongoing
- Published 2026-06-10
On 2026-06-10 the FDA classified a Class II recall of PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050 by Oculus Technologies, citing the recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material incompatibility between the produ….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2275-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-04-27 |
| Published | 2026-06-10 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Oculus Technologies |
| Distribution | US |
Product
PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
Reason
The recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material incompatibility between the product solution and the stainless steel spring and may result in visible discoloration and the presence of trace levels of metallic elements (including iron, chromium, and nickel) in the solution during use.
Identifiers
| code_info | UDI:00860009268616 Lot: 25G263 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2275-2026%22
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