Altaire Recalls TRP Blur Relief Eye Drops Due to Sterility Concerns
Altaire Pharmaceuticals is recalling TRP Blur Relief eye drops because the company cannot guarantee the product is sterile.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
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 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. 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. Per the rubric, FDA Class II recalls with potential for significant injury or hospitalization (implied by sterility failure in an ophthalmic product) map to a score of 4 (Severe), as Class I is required for score 5.
Plain-English summary
Altaire Pharmaceuticals, Inc. is recalling TRP Blur Relief, 15 mL (NDC 17312-002-11) due to a lack of assurance of sterility. The recall involves 24,144 units distributed nationwide in the United States. The affected product codes are 16256 09/19 and 17194 7/20.
The recall was initiated because the manufacturer cannot ensure that the eye drops are sterile. This classification indicates a potential risk of contamination, although the source text does not specify the type of contaminant or report any specific illnesses or injuries.
Consumers who have this product should stop using it and contact Altaire Pharmaceuticals for further instructions or a refund. The recall is classified as Class II by the FDA, indicating that use of the product could cause temporary or medically reversible health consequences.
The recalled product
- Product
- TRP Blur Relief, 15 mL, NDC 17312-002-11
- Manufacturer
- Altaire Pharmaceuticals, Inc.
- Category
- Drug — Ophthalmic
- Affected units
- 24,144
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)
- 16256 09/19 17194 7/20
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.
See all 134 products in this recall →Related recalls
Same manufacturer · Altaire Pharmaceuticals, Inc.
See all →- SevereCVS Health Dry Eye Relief Lubricant Eye Drops Recalled for Sterility Concerns
FDA (Drugs) · 2019-11-27
- SevereCVS Health Lubricant Eye Drops Recalled for Sterility Concerns
FDA (Drugs) · 2019-11-27
- SevereCVS Health Redness Relief Eye Drops Recalled for Sterility Concerns
FDA (Drugs) · 2019-11-27
- SevereAltaire Recalls Equate Support Advanced Twin Pack Due to Sterility Concerns
FDA (Drugs) · 2019-11-27
- SevereAltaire Recalls OCuSOFT Ophthalmic Ointment Due to Sterility Concerns
FDA (Drugs) · 2019-11-27
Same hazard · sterility failure
See all →- SevereAvKare Carboxymethylcellulose Sodium Eye Drops Recalled for Sterility Concerns
FDA (Drugs) · 2026-09-30
- SevereAvKare Carboxymethylcellulose Sodium Eye Drops Recalled for Sterility Concerns
FDA (Drugs) · 2026-09-30
- SevereROHTO DIGI-EYE Eye Drops Recalled Over Sterility Assurance Gap
FDA (Drugs) · 2026-07-29
- HighROHTO DRY-AID Eye Drops Recalled Due to Sterility Concerns
FDA (Drugs) · 2026-07-29
- SevereOne-Piece Introducer Tray kits recalled for sterility failure
FDA (Devices) · 2026-07-22
Similar recalls
- HighTRP Blur Relief Eye Drops Recalled Nationwide for Sterility Assurance Failure
FDA (Drugs) · 2024-03-20
- HighEye Drops Recall: TRP Eye Twitching Relief Lacks Sterility Assurance
FDA (Drugs) · 2024-03-20
- HighTRP Natural Eyes sterile eye drops recalled for lack of sterility assurance
FDA (Drugs) · 2023-09-27
- HighTRP Natural Eyes eye drops recalled due to lack of sterility assurance
FDA (Drugs) · 2024-03-20
- HighTRP Natural Eyes Allergy Relief Eye Drops Recalled for Sterility Assurance Issues
FDA (Drugs) · 2024-03-20
- HighTRP Natural Eyes Dryness Relief Eye Drops Recalled for Lack of Sterility Assurance
FDA (Drugs) · 2024-03-20