Lower riskDrug recall · FDA · Published December 30, 2020
Allergan Refresh Relieva Eye Drops: Missing Instructions for Use
Allergan recalls Refresh Relieva PF Preservative-Free Lubricant Eye Drops due to missing instructions for use. Consumers should check product labels for lot numbers and expiration dates.
“Allergan Refresh Relieva Eye Drops: Missing Instructions for Use.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36560-allergan-refresh-relieva-eye-drops-missing-instructions-for-use. Based on FDA recall #D-0233-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0233-2021%22&limit=1).
The FDA announced on Dec. 30, 2020, that Allergan, PLC. voluntarily recalled Refresh Relieva PF Preservative-Free Lubricant Eye Drops due to missing instructions for use inserts. The recall affects 100,634 bottles distributed nationwide.
How to tell if you have it
Brand: Allergan
Product: Refresh Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz (10 mL) Sterile Distributed by: Allergan, an AbbVie
UPC: 00300236634100
Lots: T0392 Exp. Jul. 2022, T0843 Exp. Aug. 2022
The hazard
The hazard is the absence of instructions for use inserts in the packaging, according to the FDA.
Context
GovInfoNow's records show Allergan, PLC. has 7 other recalls on record since May 24, 2018. Other recent recalls include the Allergan REFRESH Contact Lens Comfort Drops Recall (Dec. 29, 2020) and the Allergan Skin Medica Acne Lotion Recall (July 6, 2020). Similar products have faced issues, including Clear Eyes Eye Drops (Sept. 15, 2026), TRP Gentle Eyes Lubricant Eye Drops (Aug. 20, 2026), and Rohto Cooling Eye Drops (July 14, 2026).
How to tell if you have this one
Check the product label for the lot number (T0392 or T0843) and expiration date (July 2022 or August 2022). The product is a 0.33 fl oz (10 mL) sterile eye drop solution distributed by Allergan.
Brand
Allergan
Product
Refresh Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz (10 mL) Sterile Distributed by: Allergan, an AbbVie
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the lot number (T0392 or T0843) and expiration date (July 2022 or August 2022) on the packaging.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 2.5 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0233-2021 (December 30, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0233-2021 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 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.