FDA Device recall Z-0326-2026
Alcon PRECISION1 One-Day Contact Lenses, -2.25D
- FDA Device
- Class II
- ongoing
- Published 2025-11-05
On 2025-11-05 the FDA classified a Class II recall of Alcon PRECISION1 One-Day Contact Lenses, -2.25D by Alcon Research, citing potential for a weak seal in some units resulting in compromise in sterility.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0326-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-09-30 |
| Published | 2025-11-05 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Alcon Research |
| Distribution | AL, AR, AZ, CT, FL, IA, ID, LA, MA, MD, MI, MN, NJ, NY, OK, OR, TN, TX, WA |
Product
Alcon PRECISION1 One-Day Contact Lenses, -2.25D.
Reason
Potential for a weak seal in some units resulting in compromise in sterility.
Identifiers
| code_info | GTIN: 00730822254946; Lot Number: A8041128 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Other recalls by Alcon Research
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FDA Drug · Class II · 2026-05-06 · Alcon Research - Systane, Lubricant Eye Gel, Night Gel, Sterile, 10g (0.35 oz), Processed in France for: Alcon Laboratiroes, Inc., Fort Worth, TX 76134, USA…
FDA Drug · Class II · 2026-05-06 · Alcon Research - Brand Name: Alcon Laboratories, Inc
FDA Device · Class I · 2025-12-31 · Alcon Research - CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU/ 8065000093
FDA Device · Class II · 2025-12-03 · Alcon Research - Brand Name: Alcon Laboratories, Inc
FDA Device · Class II · 2025-11-05 · Alcon Research
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0326-2026%22
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