Oasis Tears Lubricant Eye Drops Recalled for Missing Bottle Labels
Oasis Medical Inc. is recalling 10,549 bottles of Oasis Tears Lubricant Eye Drops because the label on the immediate bottle is missing.
The agency’s classification
FDA (Drugs): Class III
Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 1/5 (Low).
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is classified as FDA Class III, which by definition is unlikely to cause adverse health consequences. The hazard is a packaging/labeling issue (missing label) without reported injuries or illnesses.
Plain-English summary
Oasis Medical Inc. is recalling 10,549 bottles of Oasis Tears, Lubricant Eye Drops, 10mL/0.3 fl. oz. Bottle, OTC Only. The product is distributed by OASIS, OASIS Medical, Inc., located in Glendora, CA. The specific lot number is OTM-07, with an expiry date of 12/2015.
The recall was initiated due to a labeling defect where the label on the immediate bottle is missing. This issue affects the product's identification and safety information visibility.
The affected product was distributed nationwide in the US. Consumers who have this product should check their bottles for the missing label and stop using the product if the label is absent.
The recalled product
- Product
- Oasis TEARS, Lubricant Eye Drops, 10mL/0.3 fl. oz. Bottle, OTC Only. Distributed by: OASIS, OASIS Medical, Inc., Glendora, CA 91741. UPC: 8 54819 00002 3.
- Manufacturer
- Oasis Medical Inc
- Category
- Drug — Ophthalmic
- Hazard
- Affected units
- 10,549
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 (2)
- Lot #: OTM-07
- Expiry: 12/2015.
Distribution
Distributed nationwide across the United States.
Related recalls
Same manufacturer · Oasis Medical Inc
See all →- SevereOasis Tears PF Lubricant Eye Drops Recalled for Sterility Assurance
FDA (Drugs) · 2026-05-20
- LowOasis Medical Recalls HPMC Visoelastic Topical Due to pH Specification Failure
FDA (Drugs) · 2015-12-30
- LowOasis Medical Recalls HPMC Visoelastic Due to Potential pH Specification Failure
FDA (Drugs) · 2015-12-30
- LowOasis Medical Recalls HPMC Visoelastic Due to pH Specification Failure
FDA (Drugs) · 2015-12-30
- LowOasis Medical Recalls ImproVue Ophthalmic Drops for pH Specification Failure
FDA (Drugs) · 2015-09-16
Same hazard · mis labeling
See all →- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-10-14
- HighJ K Patisserie Chocolate Chip Cookies Recalled for Undeclared Soy
FDA (Food) · 2026-10-14
- HighFreshPoint Recalls Cranberry Chicken Salad Wedges for Undeclared Egg Allergen
FDA (Food) · 2026-10-14
- HighJ K Patisserie & Bakery LLC Recalls Croissants for Undeclared Egg
FDA (Food) · 2026-10-14
- LowMindray ePM Series Patient Monitor Manuals Recalled for Alarm Clarification
FDA (Devices) · 2026-10-14
Similar recalls
- SevereOasis Tears PF Lubricant Eye Drops Recalled for Sterility Assurance
FDA (Drugs) · 2026-05-20
- SevereOCuSOFT Tears Again Lubricant Eye Drops Recalled for Sterility Concerns
FDA (Drugs) · 2019-11-27
- HighCVS Health Natural Tears Lubricant Eye Drops Recalled for Sterility Concerns
FDA (Drugs) · 2019-11-27
- ModerateCell Distributors Recalls Refresh Tears Eye Drops for Labeling Defects
FDA (Drugs) · 2017-05-31
- SevereAltaire Recalls Ocusoft Tears Again Lubricant Eye Drops Due to Sterility Concerns
FDA (Drugs) · 2019-11-27
- SevereArtificial Tears Eye Drops Recalled for Manufacturing and Sterility Issues
FDA (Drugs) · 2025-05-14