FDA Device recall Z-1956-2025
Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution
- FDA Device
- Class II
- ongoing
- Published 2025-06-18
On 2025-06-18 the FDA classified a Class II recall of Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution by Contamac Solutions, citing contact lens insertion solution may lack sterility.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1956-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-05-15 |
| Published | 2025-06-18 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Contamac Solutions |
| Distribution | US |
Product
Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution
Reason
Contact lens insertion solution may lack sterility.
Identifiers
| code_info | UDI: 00850012123002/ Lot: HFH, HGC, HGI, HGN, HKF, HKK |
|---|
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-1956-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.