Class II · Moderate risk
Pluvicto
CGMP deviations
Is Willow recalled?
Yes — there is an active recall. 5 ongoing FDA recalls mention Willow (7 total). Check the affected lots below.
Most common reason: Failed specification (4 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Willow. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Willow recalls on record
none so far in 2026; 7 on record, newest first
Class II · Moderate risk
Natural Pain Relieving Cream
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Class II · Moderate risk
Natural Pain Relieving Cream
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Class II · Moderate risk
Natural Pain Relieving Cream
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Class II · Moderate risk
Natural Pain Relieving Cream
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Class III · Low risk
Pluvicto 1
Labeling: Incorrect or Missing Lot and/or Exp Date: vials were labeled with the incorrect lot number and expiration date
Class II · Moderate risk
Midazolam 1 mg/mL
Lack of Assurance of Sterility: Potential leakage of bags.
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.