---
title: Medline Industries, LP — FDA recall record
license: CC0-1.0
source: openFDA drug & device recall enforcement records — U.S. FDA
---

# Medline Industries, LP — FDA recall record

The FDA recall enforcement history of Medline Industries, LP: 351 recalls (68 Class I), drug/device split, severity mix, recurring reasons, and ongoing count. RECORDED openFDA records, keyed by the exact firm name. Not a quality verdict or medical advice. CC0.

## Claims

### Medline Industries, LP has 351 FDA recalls on record (2025–2026)

**DERIVED.** Medline Industries, LP has 351 FDA recall enforcement records (2 drug, 349 device), of which 68 are Class I (the FDA's most-serious tier), 282 Class II, 1 Class III; 351 are ongoing. An AGGREGATED count of openFDA enforcement records keyed by firm name (occurred=true; adjudged=FALSE — the Atlas counted them, the FDA published the records).

Source: openFDA drug & device 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 & device 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 count is not a quality verdict

**INTERPRETATION.** A recall count is not a quality verdict — large firms recall more by volume and most recalls are voluntary; the Class I count and ongoing status are the signal, not the raw total. Keyed by the exact firm-name string (a large firm may file under variants; see the FDA recall database for the complete cross-variant record). Not medical advice.

Source: Drug & Device Safety Atlas L5 boundary (recall count ≠ quality verdict) — 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/firm/medline-industries-lp.jsonld`

## Data

### FDA recall summary — Medline Industries, LP

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

| Metric | Value | Status |
| --- | --- | --- |
| Total recalls | 351 | aggregated |
| Drug recalls | 2 | aggregated |
| Device recalls | 349 | aggregated |
| Class I (most serious) | 68 | aggregated |
| Class II | 282 | aggregated |
| Class III | 1 | aggregated |
| Ongoing | 351 | aggregated |
| Year span | 2025–2026 | aggregated |
| Top reason #1 | Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All pro (84×) | aggregated |
| Top reason #2 | During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sp (31×) | aggregated |