Drug & Device Safety Atlas

FDA drug recalls · openFDA

Is POVIDONE-IODINE recalled?

The FDA has recorded 2 recalls of POVIDONE-IODINE (2024–2025) , recalled under brands like FIRST AID ANTISEPTIC, POVIDONE-IODINE. 2 still ongoing.

0
Class I (most serious)
1
Class II
1
Class III
2
ongoing

A recall doesn't mean your pills are affected

Drug recalls are issued by lot (specific batches, identified by lot numbers / NDC) — not for every bottle of POVIDONE-IODINE ever made. To know if yours is involved, match the lot codes on the recall below against your bottle, or ask your pharmacist. Do not stop a prescribed medication because of a recall without talking to your pharmacist or prescriber — stopping can be more dangerous than the recall. The Class is the FDA's risk judgment (Class I = reasonable probability of serious harm or death), not a measurement that harm occurred; most recalls are voluntary and Class II/III.

Why it was recalled

Incorrect/Undeclared Excipients: The inactive ingredients labeled on the product boxes and tubes are listed as "mineral 1
Subpotent drug 1

The recalls

Class I and ongoing recalls first. Tap a recall for its full record and lot detail.

RECORDED — these are the FDA's published recall enforcement records (openFDA), grouped by the generic drug name. Scope: drug recalls the FDA recorded with a generic name; device recalls and recalls without a generic name are in the full recall browse. "Ongoing" reflects openFDA's last-published status — confirm current status and your lot at the FDA recall database. This page informs and routes; it is not medical advice.

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