Prestige Brands Holdings CLEAR EYES Maximum Itchy Eye Relief Recall
Announced 2026-08-19 · FDA
Recall involves Prestige Brands Holdings’ CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, distributed nationwide in the USA. The recall is due to lack of assurance of sterility and potential contamination, per FDA notice. About 39,060 bottles (Lot 2552A, Exp 09/30/2027) are affected.
| Brand | Prestige Brands Holdings |
|---|---|
| Product | CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY 10591, a Prestige Consumer Healthcare Company. NDC: 67172-999-01 UPC 6 78112 65920 3 |
| Reason | Lack of assurance of sterility. The recall is due to potential contamination |
| Severity | moderate |
| Units affected | 39060 |
| Distribution | Nationwide in the USA. |
| Agency | FDA |
WHAT YOU SHOULD DO
- Stop using the recalled eye drops immediately and discard any bottles you have.
- Discard any bottle with Lot 2552A (Exp 09/30/2027) and keep the packaging for reference.
- Contact Prestige Brands Holdings for refund or replacement and follow any recall instructions from the distributor, Medtech Products Inc.
- If you have experienced adverse effects, consult a healthcare professional and report the issue to FDA MedWatch.
How to identify the recalled item
| Lot / date codes | Lot 2552A, Exp 09/30/2027 |
|---|---|
| Lot / date codes | Lot 2552A, Exp 09/30/2027 |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.