RECALL DATABASE

Eye Drops Recall: Oasis Tears PF

Announced 2026-05-20 · FDA

Lack of assurance of sterility prompted the recall of Oasis Tears PF preservative-free lubricant eye drops distributed nationwide in the United States. The recall covers Lot # 1V59 (exp 05/31/26) and Lot # 3V12, 3V69 (exp 08/31/26) following FDA observations during an inspection. No corrective action is specified in the provided recall notice.

BrandOasis Medical, Inc.
ProductOasis Tears PF, Preservative-Free Lubricant Eye Drops, 10mL/0.34 Fl OZ Bottle, Sterile, Manufactured for: OASIS Medical, Inc., 514 S. Vermont Ave., Glendora, CA 91741, USA, Made in France, NDC 42126-6400-1.
ReasonLack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations noted during a recent inspection of Excelvision.
Severitymoderate
DistributionNationwide within the United States
AgencyFDA

WHAT YOU SHOULD DO

  1. Check your Oasis Tears PF bottle for Lot 1V59 (exp 05/31/26) or Lot 3V12/3V69 (exp 08/31/26) and stop use if you have a recalled lot.
  2. Do not use the recalled eye drops and keep them away from children.
  3. Contact Oasis Medical, Inc. for return/replacement instructions or refunds.
  4. If you have symptoms after using the product, seek medical advice.

How to identify the recalled item

Lot / date codesLot # 1V59, Exp Date: 05/31/26; Lot # 3V12, 3V69, Exp Date: 08/31/26.
Lot / date codesLot # 1V59, Exp Date: 05/31/26; Lot # 3V12, 3V69, Exp Date: 08/31/26.

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.