PlainRecalls

Medline Industries, LP - Northfield

Compiled from official public sources by the editorial team.

822 recalls on record · Latest: Oct 1, 2025

Medline Industries, LP - Northfield Recall Insight

Medline Industries, LP - Northfield appears on 822 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.808% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Oct 1, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 22 entries, severity tagging shows 0 critical, 22 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 22 of 22 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (22). The date window on this page runs from Dec 29, 2021 to Oct 5, 2022.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Oct 5, 2022

MEDLINE CLEARPRO TRACH T-PIECE CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner cartons per Case (CS). Labele…

FDA Devices Moderate Oct 5, 2022

MEDLINE CLEARPRO TRACH DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner cartons per Case (CS). …

FDA Devices Moderate Oct 5, 2022

MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner cartons per Case (CS). Labele…

FDA Devices Moderate Aug 10, 2022

MEDLINE MICRO-KILL GERMICIDAL BLEACH WIPES, Model numbers MSC351420AN, MSC351420ANH, MSC351420ANZ, MSC351430A, MSC351430AZ

FDA Devices Moderate Jul 6, 2022

Medline Pill Splitters; 1 each/box; 144 boxes/carton

FDA Devices Moderate Jun 8, 2022

MEDLINE Polyurethane Foam Bedside Cleaning Kit, REF DYK500FS

FDA Devices Moderate Jun 8, 2022

MEDLINE Polyurethane Bedside Cleaning Kit, REF DYK500FSAW

FDA Devices Moderate Jun 8, 2022

MEDLINE Polyurethane Foam Bedside Cleaning Kit, REF DYK215FS

FDA Devices Moderate Jun 8, 2022

MEDLINE Polyurethane Foam Bedside Cleaning Kit, REF DYK100FS

FDA Devices Moderate Jun 8, 2022

MEDLINE Polyurethane Foam Enzymatic Cleaning Sponge, REF DYK1000TSE

FDA Devices Moderate Jun 1, 2022

ABX Pentra Calcium AS CP, Reagent 90 mL, REF A11A01954

FDA Devices Moderate Apr 20, 2022

Medline Standard PVC Laryngeal Masks, 1 device per pouch, 5 each pouches per box

FDA Devices Moderate Apr 20, 2022

Stanbio TDM/Beta-Hydroxybutyrate Linearity Standards, packaged in boxes containing Levels 1-6, 1 x 4 mL each, REF 2450-604, Medline catalog number S-…

FDA Devices Moderate Apr 20, 2022

Hydroxybutyrate LiquiColor Tests - includes 3 bottles (1 of each size, 3mL, 8.5mL, and 50mL)

FDA Devices Moderate Apr 13, 2022

Excelsior Medical 10mL Sterile Field Saline Flush ZR, 0.9% Sodium Chloride Injection, USP, REF EMZ10091280, Sterile, IV Flush Only, Contents of Packa…

FDA Devices Moderate Mar 9, 2022

MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes

FDA Devices Moderate Mar 2, 2022

meridian bioscience immunocard STAT! Rotavirus test, REF 750030, 30 tests/kit box. The ImmunoCard STAT! Rotavirus Immunoassay is a rapid in vitro qu…

FDA Devices Moderate Mar 2, 2022

Michels Transport Medium, 20ML Prefilled Cont

FDA Devices Moderate Feb 16, 2022

CURAD REUSABLE GEL HOT/COLD PACK

FDA Devices Moderate Feb 9, 2022

HARDY DIAGNOSTICS CatScreen, 25dsk/vial

FDA Devices Moderate Feb 9, 2022

Premier Rotaclone, Rx only

FDA Devices Moderate Dec 29, 2021

Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls, Ref. No. 2460-605

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.