Altaire Recalls Up & Up Lubricating Eye Drops for Sterility Concerns
Altaire Pharmaceuticals is recalling Up & Up Intensive Relief Lubricating Eye Drops due to a lack of assurance of sterility.
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 and involves a lack of assurance of sterility in an ophthalmic product, which poses a significant risk of serious injury or infection, meeting the criteria for a Severe rating.
Plain-English summary
Altaire Pharmaceuticals, Inc. is recalling specific lots of TRP/ TARGET up & up intensive relief lubricating eye drop, 10 mL. The recall was initiated because of a lack of assurance of sterility in the product.
The affected product is distributed nationwide in the United States. The recall covers specific lot codes 17290 9/19 and 18052 2/20.
Consumers should stop using the recalled eye drops and contact their healthcare provider or the recalling firm for further instructions.
The recalled product
- Product
- TRP/ TARGET up & up intensive relief lubricating eye drop, 10 mL
- Manufacturer
- Altaire Pharmaceuticals, Inc.
- Category
- Drug — Ophthalmic
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)
- 17290 9/19 18052 2/20
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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