RECALL DATABASE

Drops Recall: Scope Health Optase Dry Eye

Announced 2026-05-06 · FDA

FDA recall of Optase Dry Eye Intense Drops due to lack of assurance of sterility. The recall covers multiple lots (8T98, 9T31, 9T32, 2V13, 2V14, 2V15, 3V35, 3V36, 3V37, 5V45, 5V46, 9V12, 1X57, 1X70, 1X84) with expiry dates through 2027, distributed nationwide in the United States. Consumers should check their lot numbers and stop using any recalled product.

BrandSCOPE HEALTH
ProductOptase Dry Eye Intense Drops (Glycerin 0.2%), packaged in 0.33 fl oz, Sterile, Manufactured for Scope Health Inc., 79 Madison Ave., 8th Floor, New York, NY 10016, USA, NDC 72972-002-01.
ReasonLack of Assurance of Sterility
Severitymoderate
DistributionNationwide within the United States
AgencyFDA

WHAT YOU SHOULD DO

  1. Check your bottle's lot number against the recalled lots and stop using any that match.
  2. Do not use the affected product; dispose of it or return it to the retailer.
  3. If you have used the product or have symptoms, contact your healthcare provider.
  4. Visit the FDA recall page or Scope Health customer service for more information.

How to identify the recalled item

Lot / date codesLot#: 8T98, 9T31, 9T32, Exp. Date: 30/04/26; 2V13, 2V14, 2V15, Exp. Date 30/06/26; 3V35, Exp. Date 31/08/26;3V36, 3V37, Exp. Date 30/09/26; 5V45, 5V46, 9V12, Exp. Date 31/03/27; 1X57, 1X70, 1X84, Exp. Date 31/05/27.
Lot / date codesLot#: 8T98, 9T31, 9T32, Exp. Date: 30/04/26; 2V13, 2V14, 2V15, Exp. Date 30/06/26; 3V35, Exp. Date 31/08/26;3V36, 3V37, Exp. Date 30/09/26; 5V45, 5V46, 9V12, Exp. Date 31/03/27; 1X57, 1X70, 1X84, Exp. Date 31/05/27.

These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.

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This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.