CLASS III Drug recall · Reported 16 Sep 2015 · FDA Enforcement Report
ImproVue Ophthalmic Lubricant Drops recalled by Oasis Medical
Oasis Medical is recalling ImproVue Ophthalmic Lubricant Drops (1.7% Hypromellose) Use Syringe Use Applicator Tip per, distributed in Florida. The recall was initiated on 31 Aug 2015 and the FDA has classified it as Class III.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1418-2015
- FDA event ID
- 72111
- Recalling firm
- Oasis Medical, Glendora, CA
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 31 Aug 2015
- FDA classified
- 9 Sep 2015
- Reported
- 16 Sep 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Other Reasons
- Drug class
- Eye Drops
Timeline
| 31 Aug 2015 | Recall initiated by company | |
| 9 Sep 2015 | Classified by FDA | +9 days |
| 16 Sep 2015 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Falied pH specification
Product as listed by the FDA
ImproVue Ophthalmic Lubricant Drops (1.7% Hypromellose), 1 Single Use Syringe, 0.07 fl oz (2mL), 1 Single Use Applicator Tip per carton, Manufactured for OCULUS SURGICAL, Port St. Lucie, FL 34986, NDC 62144-5510-05
Where it was distributed
FL
Questions about this recall
Why was it recalled?
Falied pH specification
Which lots are affected?
Lot # V0415F, Exp 10/16
Where was it sold?
FL
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Oasis Medical
All 7| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Oasis Tears PF, Preservative-Free Lubricant Eye Drops/, Sterile recalledOasis Tears Pf | Oasis Medical | Sterility | Nationwide |
| Drug | CLASS III | HPMC Visoelastic, 20,000 cps, Reference recalled by Oasis Medical | Oasis Medical | Other | Nationwide |
| Drug | CLASS III | Hpmc Visoelastic, 8,000 cps, Reference 51082, LT5108 recalled | Oasis Medical | Other | Nationwide |
| Drug | CLASS III | Hpmc Visoelastic Topical, 8,000 cps, Reference recalled by Oasis Medical | Oasis Medical | Other | Nationwide |
| Drug | CLASS III | ImproVue Ophthalmic Lubricant Drops recalled by Oasis Medical | Oasis Medical | Other | FL |