CVS Health Redness Relief Eye Drops Recalled for Sterility Concerns
Altaire Pharmaceuticals is recalling CVS Health Redness Relief Eye Drops due to a lack of assurance of sterility. Consumers should stop using the product and return it to the pharmacy.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II, which corresponds to a 'Severe' rating under the rubric. The hazard involves a lack of assurance of sterility in an ophthalmic product, posing a significant risk of infection.
Plain-English summary
Altaire Pharmaceuticals, Inc. is recalling CVS Health Redness Relief Lubricant Redness Reliever Eye Drops, Sterile, 0.5 fl. oz. (15 mL), Item #317912. The recall is being conducted because of a lack of assurance of sterility in the product.
The affected product was distributed nationwide in the United States by CVS Pharmacy Inc. The recall covers 464,424 units. Specific lot numbers and expiration dates are listed in the official recall notice.
Consumers who have purchased this product should stop using it immediately. They should return the product to the pharmacy where it was purchased for a refund or follow the instructions provided by the recalling firm.
The recalled product
- Product
- CVS Health Redness Relief Lubricant Redness Reliever Eye Drops, Sterile, 0.5 fl. oz. (15 mL), Item #317912, Distributed by: CVS Pharmacy Inc., One CVS Drive, Woonsocket, RI 02895
- Manufacturer
- Altaire Pharmaceuticals, Inc.
- Category
- Drug — Ophthalmic
- Affected units
- 464,424
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot #: 18229 9/21 18031 1/21 17131 5/20 17059 3/20 17008 1/20 19056 03/22
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 134 recalled by Altaire Pharmaceuticals, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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