Skip to content
Use caution Drug recall · FDA · Published April 10, 2015

Oasis Medical Recalls ImproVue Eye Drops Over pH Issues

Oasis Medical recalls ImproVue Ophthalmic Lubricant Drops due to failed pH specifications. Check lot numbers V0814B and V1014H.

🇺🇸 FDA recall #D-1084-2015DrugOasis Medical ›
Take action

Contact the company

Recalling firmOasis Medical, Inc.514 S Vermont Ave Bldg 510-528 · Glendora, CA 91741-6205
✎ GovInfoNow plain-language explainer

Oasis Medical, Inc. is recalling ImproVue Ophthalmic Lubricant Drops because they failed pH specification requirements. The recall affects 9,731 cartons distributed in Florida. Specific lots include V0814B (expiring 02/16) and V1014H (expiring 04/16). Read more at govinfonow.com/recall/44808-oasis-medical-inc-recalls-improvue-ophthalmic-lubricant-drops-1-7.

Source Summary by GovInfoNow · govinfonow.com/recall/44808-oasis-medical-inc-recalls-improvue-ophthalmic-lubricant-drops-1-7 · Updated October 12, 2026 · FDA enforcement record: FDA #D-1084-2015

Cite this page

“Oasis Medical Recalls ImproVue Eye Drops Over pH Issues.” GovInfoNow, updated October 12, 2026. https://govinfonow.com/recall/44808-oasis-medical-inc-recalls-improvue-ophthalmic-lubricant-drops-1-7. Based on FDA recall #D-1084-2015 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1084-2015%22&limit=1).

The FDA announced on April 10, 2015, that Oasis Medical, Inc. is recalling ImproVue Ophthalmic Lubricant Drops due to a failed pH specification. The recall affects 9,731 cartons distributed in Florida.

How to tell if you have it

  • Brand: Oasis Medical
  • Product: ImproVue Ophthalmic Lubricant Drops (1.7% Hypromellose)
  • Size: 0.07 fl oz (2mL) Single Use Syringe
  • NDC: 62144-5510-05
  • Lot Codes: V0814B, Exp 02/16; V1014H, Exp 04/16
  • Distribution: Florida

The hazard

The product failed to meet pH specifications. The recall is classified as Class III.

Context

GovInfoNow's records show Oasis Medical, Inc. has four other recalls on file since May 14, 2014. Other recent recalls of similar products include PRED MILD Eye Drops (May 18, 2026), Ciclopirox Shampoo 1% (Dec. 9, 2025), and Fluocinolone Acetonide Solution (Dec. 30, 2025).

How to tell if you have this one

Check your ImproVue Ophthalmic Lubricant Drops for lot numbers V0814B or V1014H. The product is manufactured for OCULUS SURGICAL in Port St. Lucie, FL, and carries NDC 62144-5510-05.

  • Brand
    Oasis Medical
  • Category
    Drug

Where it went and when

Where it was distributed

Distributed in Florida.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “FL” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida.

Recall timeline

FDA terminated this recall 8 months after the firm started it.

1. Firm started the recall: Apr 10, 201512. FDA classified it Class III: May 21, 201523. Published in FDA’s Enforcement Report: May 27, 201534. FDA terminated the recall: Dec 18, 201542015
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

Similar recalls

Latest drug recalls

Keep exploring

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-1084-2015 (April 10, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1084-2015 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 12, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA