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 50 entries, severity tagging shows 10 critical, 40 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 46 of 50 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 3 distinct product categories, with issuing agencies dominated by FDA Devices (48), FDA Drug (2). The date window on this page runs from Aug 9, 2023 to Mar 6, 2024.

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 Critical Mar 6, 2024

MEDLINE BRONCHOSCOPY TRAY, REF DYNDL1350A

FDA Devices Critical Mar 6, 2024

MEDLINE ARTERIAL BUNDLE NO CATHETER, REF ART995

FDA Devices Critical Mar 6, 2024

MEDLINE kits and trays, labeled as: a) SUCTION CATH 10FR KIT W/SALINE, REF DYND41470SA, DYND41470SAH; b) TRACH CARE TRAY, REF DYNDA1931B, DYNDA19…

FDA Devices Critical Mar 6, 2024

MEDLINE Kits, trays, and packs labeled as follows: a) Description, REF DYNDH1679; b) BREAST BIOPSY TRAY, REF DYNDH1664; c) BREAST BIOPSY TRAY,…

FDA Devices Critical Mar 6, 2024

Medline Kits, trays, and packs labeled as follows: a) BREAST PACK, REF DYNJ56344B; b) SEPTOPLASTY PACK WRO-LF, REF DYNJ62803

FDA Devices Critical Mar 6, 2024

Centurion Kits, trays, and packs labeled as follows: LACERATION TRAY, REF ST11670A

FDA Devices Moderate Feb 28, 2024

These wipes are saturated with 0.65% bleach solution. These wipes are antimicrobial, disinfectant with sporicidal, virucidal, bactericidal, and fungi…

FDA Drug Moderate Feb 14, 2024

Medline Remedy Clinical TREAT Antifungal Cream, 2% Miconazole Nitrate, Paraben Free, 4 FL OZ (118 mL) tube, Manufactured for Medline Industries, LP T…

FDA Devices Moderate Feb 7, 2024

MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1723

FDA Devices Moderate Feb 7, 2024

MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1622C

FDA Devices Moderate Feb 7, 2024

MEDLINE BLOOD CULTURE COLLECTION KIT, Reorder Number DYNDH1714A

FDA Devices Moderate Feb 7, 2024

MEDLINE BLOOD CULTURE BOTTLE KIT, Reorder Number DYNDH1738A

FDA Devices Moderate Feb 7, 2024

MEDLINE ADULT BLOOD CULTURE KIT, Reorder Number DYNDH1694A

FDA Devices Moderate Feb 7, 2024

MEDLINE BLOOD CULTURE TRAY ADULT, Reorder Number DYNDH1194A

FDA Devices Moderate Feb 7, 2024

MEDLINE BLOOD CULTURE COLLECTION KIT, Reorder Number DYNDH1626B

FDA Devices Moderate Jan 17, 2024

Medline Gown Poly W/Breath Sleeves XL AAMIK Level 4 (Eclipse gown), REF SPT-2208CS, 100/pack, Non-Sterile.

FDA Devices Critical Jan 3, 2024

Tracheostomy care kits: (1) Medline Tracheostomy Clean and Care Tray with 14 Fr Suction Catheter, REF DYND40580, Sterile; (2) Medline Tracheost…

FDA Devices Critical Jan 3, 2024

(1) Nursing Skills kit, SKU #EDUC05038B, Case UPC 40195327019878, Non-sterile, For Training Purposes Only, Not For Human Use.

FDA Devices Critical Jan 3, 2024

(1) Nurse Kit, SKU #EDUC1025, Case UPC 40195327196647, Non-sterile, For Training Purposes Only, Not For Human Use.; and (2) Nursing Tote Kit, SKU #E…

FDA Devices Moderate Dec 20, 2023

STERILE PVP SOLUTION, REF DYNDA1907

FDA Devices Moderate Dec 20, 2023

Medline Leg bag, REF URO12573

FDA Devices Moderate Dec 20, 2023

STERILE POVIDONE, REF DYNDA2061

FDA Devices Moderate Dec 20, 2023

Medline Leg bag, REF DYND12574

FDA Devices Moderate Dec 20, 2023

STERILE BETADINE, REF DYNDA1998

FDA Devices Moderate Dec 20, 2023

Medline Leg bag, REF DYND12578

FDA Devices Moderate Dec 20, 2023

STERILE PVP, REF DYNDA1649

FDA Devices Moderate Dec 20, 2023

STERILE STERILE PREP STICK, REF DYNDA1134

FDA Devices Moderate Dec 20, 2023

STERILE PVP SLN KIT, REF DYNDM1097

FDA Devices Moderate Dec 20, 2023

PVP SOLUTION SING STRL, REF DYNDA1858

FDA Devices Moderate Nov 22, 2023

ADLT BLOOD CULTURE COLLECT KIT, REF DYNDH1245

FDA Devices Moderate Nov 22, 2023

PERIPHERAL BLOOD CULTURE DRAW, REF DYNDH1561

FDA Devices Moderate Nov 22, 2023

BLOOD CULTURE KIT, REF DYNDH1647B

FDA Devices Moderate Nov 22, 2023

24 BLOOD CULTURE KIT, REF DYNDH1632

FDA Devices Moderate Nov 22, 2023

CENTRAL LINE BLOOD CULTURE DRA, REF DYNDH1562

FDA Drug Moderate Nov 15, 2023

Clinical TREAT Antifungal Powder, Vanilla Scent, 3 OZ (85 g) tube, Active Ingredient: Miconazole Nitrate 2.0% w/w Antifungal, Manufactured for Medlin…

FDA Devices Moderate Oct 25, 2023

MEDLINE ReNewal Harmonic ACE+7 Shears w/ Adv. Hemostasis Use Only w/ GEN11 SW v2018-1 and Lower, REF HARH45R. surgical instrument.

FDA Devices Moderate Oct 25, 2023

MEDLINE ReNewal Ligasure Maryland Jaw Sealer/Divider Nano-Coated Complatible with FT10 Generator, REF LF1944CR. electrosurgical instrument

FDA Devices Moderate Oct 25, 2023

MEDLINE ReNewal Ligasure Sealer/Divider Nano-Coated Compatible with FT10 Generator, REF LF4418CR. electrosurgical instrument

FDA Devices Moderate Oct 25, 2023

MEDLINE ReNewal Ligasure Blunt Tip Sealer/Divider Nano-Coated Compatible with FT10 Generator, REF LF1844CR. electrosurgical instrument

FDA Devices Moderate Oct 11, 2023

Centurion Sterile CirClamp with 1.45cm Bell Reprocessed, Reorder CR3145K, 1 per package, 12 per case.

FDA Devices Moderate Sep 27, 2023

MEDLINE STERILE IRIS SCISSORS CVD/STD, REF DYNJ04049

FDA Devices Critical Sep 20, 2023

HUDSON RCI Addipak, UNIT DOSE VIALS, 5mL Sterile 0.9% NaCl Solution for Inhalation USP. REF RHUD59U

FDA Devices Moderate Aug 16, 2023

Total Hip Kit, REF DYNJ903275S; surgical convenience kit

FDA Devices Moderate Aug 9, 2023

Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. A V FISTULA, Model Number: DYNJ6571…

FDA Devices Moderate Aug 9, 2023

Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. PROBE COVER PACK, Model Number: D…

FDA Devices Moderate Aug 9, 2023

Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. PEDIATRIC CATH ANGIO PACK, Model Nu…

FDA Devices Moderate Aug 9, 2023

Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. EGG RETRIEVAL PACK, Model Number:…

FDA Devices Moderate Aug 9, 2023

Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. SHY IR PICC PACK, Model Number: D…

FDA Devices Moderate Aug 9, 2023

Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. C V MINOR PACK, Model Number: DYN…

FDA Devices Moderate Aug 9, 2023

Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. ANGIOGRAPHY PACK, Model Number: D…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Medline Industries, LP - Northfield with Zimmer Biomet, Inc. →

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.