FDA-Drug2026-06-03Class IIICHEMICAL

AbbVie PRED MILD eye drops recalled for failed stability specifications

OTHERNationwide distributionDrugsAllergens

What this means

AbbVie is recalling specific lots of PRED MILD (prednisolone acetate) eye drops because they failed stability testing. The affected product may not maintain its intended strength or safety over time. Two lots are involved, with an expiration date of August 2026.

  • Check if you have PRED MILD with lot number 402805 or 407596.
  • If you do, contact your pharmacy or doctor before using it.
  • Do not discard the bottle; your pharmacist can help you return it safely.
The agency's original wording
Hazard

Failed Stability Specifications

Intended for
Adults
Illnesses reported
None reported
Sold states
US Nationwide.
Affected count
2,736 bottles
Manufactured in
1 N Waukegan Rd, North Chicago, IL, United States
Products
PRED MILD, prednisolone acetate ophthalmic suspension, USP, 0.12%, 10 mL, Sterile, Rx only, Allergen, Inc., an AbbVie company, North Chicago, IL 60064, Product of France, NDC 11980-174-10.

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0551-2026

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