---
title: TIMOLOL — FDA recall record
license: CC0-1.0
source: openFDA drug recall enforcement records — U.S. FDA
---

# TIMOLOL — FDA recall record

All 1 FDA recalls of TIMOLOL on record (0 Class I, 0 ongoing), with the severity mix, recurring reasons, brands, and per-recall lot detail. An AGGREGATED count of openFDA records grouped by generic name. A recall is by lot — a generic match is not a verdict on a specific patient's medication. Not medical advice. CC0.

## Claims

### The FDA has recorded 1 recall of TIMOLOL (2024)

**DERIVED.** TIMOLOL has 1 FDA recall enforcement records, of which 0 are Class I (the FDA's most-serious tier), 1 Class II, 0 Class III; 0 are ongoing. An AGGREGATED count of openFDA enforcement records grouped by generic name (occurred=true; adjudged=FALSE — the Atlas grouped/counted them, the FDA published the individual records).

Source: openFDA drug recall enforcement records — U.S. FDA — https://open.fda.gov/
Falsifier: occurred=TRUE: a faithful COUNT/SUM/total over the named record set that introduces NO modeling choice — it IS the case in the record. adjudged=FALSE: Atlas Commons computed the aggregate; openFDA drug recall enforcement records — U.S. FDA published the underlying records, NOT this figure. Re-count it from the named source to verify. Distinct from a median/ratio/index (which picks a population, weighting, denominator, or threshold — a constructed statistic → 'derived', occurred=FALSE) and from an authority-published total (→ 'recorded', adjudged=TRUE).

### A recall of TIMOLOL does not mean a given patient's medication is affected

**INTERPRETATION.** Drug recalls are issued by LOT (specific batches identified by lot numbers / NDC), not for all TIMOLOL. To determine whether a specific supply is affected, match the lot codes on the individual recall record against the product, or consult a pharmacist. This is not medical advice, and a recall is not a reason to stop a prescribed medication without consulting a prescriber.

Source: Drug & Device Safety Atlas L5 boundary (a recall is by lot, not by generic) — https://drug-device-safety-atlas.ryanjhunter.workers.dev/
Falsifier: occurred=FALSE (a framing, not an event) and adjudged=FALSE (an in-house reading, not an authority's verdict) — the LOWEST-warrant claim here. A flat representation would render this identically to the official facts; the four-status does not.

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Every claim above carries a four-status warrant (RECORDED / MODELED / DERIVED / INTERPRETATION) and a named source you can re-fetch — this is a research object, not a flat fact. Structured: `https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/drugs/timolol.jsonld`

## Data

### FDA recall summary — TIMOLOL

Aggregated counts of openFDA enforcement records grouped by generic name (occurred=true, adjudged=false — Atlas grouped/counted; FDA published the records). Source: openFDA.

| Metric | Value | Status |
| --- | --- | --- |
| Total recalls | 1 | aggregated |
| Class I (most serious) | 0 | aggregated |
| Class II | 1 | aggregated |
| Class III | 0 | aggregated |
| Ongoing | 0 | aggregated |
| Firms involved | 1 | aggregated |
| Year span | 2024–2024 | aggregated |
| Top reason #1 | Lack of Assurance of Sterility: Out of specification for volume and compromised container closure. (1×) | aggregated |