PlainRecalls

Medline Industries, LP - Northfield

822 recalls on record · Latest: Oct 1, 2025

Subscribe to new Medline Industries, LP recalls (RSS)

Agency notice ledger

Federal filing book Medline Industries, LP HEAVY-BOOK · MULTI-AGENCY

#2 of 14,151 · 822 notices · 0.787% archive

  • BOOK 822 notices
  • RANK #2 of 14,151
  • SHARE 0.787% archive
  • AGENCY FDA Devices (812)
  • CAT medical devices
  • CATS 3 categories
  • LATEST Oct 1, 2025
  • PHOTO Siemens Medical Solut…

Nearest notice-volume peer: Siemens Medical Solutions USA, Inc (26 notice gap)

Medline Industries, LP - Northfield sits #2 of 14,151 (2nd among 14,151 firms) with 822 federal notices — about 0.787% of the archive (heavy-book tercile). Rank counts issuance frequency, not danger. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Medline Industries, LP's standing among 14,151 recalling firms

Medline Industries, LP - Northfield ranks 2nd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Medline Industries, LP vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

822 2nd of 14151 higher than 14,149 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-14

Medline Industries, LP in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Medline Industries, LP - Northfield carries 822 distinct federal notices, ranked #2 of 14,151 (heavy-book).

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026

How the 822 notices break down

Same federal filing book as the hero total — split by issuing agency, no new counts.

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, DYNDA1931BH

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, REF DYNDH1431A; d) BREAST BIOPSY TRAY, REF DYNJ46448; e) BREAST BIOPSY TRAY, REF DYKE1520B; f) COLON KIT- BERLIN, REF DYNDH1808;

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 fungicidal activites. MEDLINE MICRO-KILL Bleach GERMICIDAL BLEACH WIPES: a) MSC351400AN/Z (7 X 8 , 150 ct canister), b) MSC351410AN/Z (6 x 5 , 150ct canister), c) MSC3560012 (private-labeled 6 x 5 , 150ct canister), d) MSC351450AN (12" x 12", 110ct bucket), e) MSC351450BG4 (12" x 12", 110ct bag)

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 Three Lakes Drive, Northfield, IL 60093. NDC: 53329-147-44

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 Tracheostomy Clean and Care Tray, REF DYND4061030, Sterile; (3) Medline Basic Tracheostomy Care Kit, REF CC3T4691A, Sterile; (4) Medline Tracheostomy Care Kit with Glove, REF CC4681A, Sterile; (5) Medline Mini Tracheostomy Care Kit, REF CC3T3030A, Sterile; and (6) Medline Mini Tracheostomy Care Kit, REF DYND40622, Non-sterile.

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 #EDUC5056A, Case UPC 40195327153695, Non-sterile, For Training Purposes Only, Not For Human Use.

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 Medline Industries, LP, Three Lakes Drive, Northfield, IL 60093 USA, NDC: 53329-169-79

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: DYNJ65711; b. ACCESS CATHETER, Model Number: DYNJ64141A; c. ACCESS PICC PACK, Model Number: DYNJ40682B; d. ADULT EPIV INSERTION TRAY, Model Number: DYNDA2482; e. AFCH CVC INSERTION, Model Number: DYNJ67534; f. ANGIOGRAM-DECH-LF, Model Number: DYNJ81725; g. ART LINE KIT ICH OR, Model Number: ART900; h. ARTERIAL LINE PACK, Model Numb

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: DYNDA1219

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 Number: DYNJ54755B; b. PEDIATRIC MAX BARRIER KIT-LF, Model Number: DYNJ40306A; c. PERC PACK-LF, Model Number: DYNJ0774759P; d. PERCUTANEOUS VASCULAR CDS, Model Number: DYNJ902261D; e. PERIPHERAL NERVE BLOCK KIT/P, Model Number: DYNJRA1747; f. PERIPHERAL PACK, Model Number: DYNJ44960D; g. PERIPHERAL ULTRASOUND CATHETER, Model Number:

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: DYNJ66291B; b. FETAL SURGERY CDS-LF, Model Number: CDS840214P; c. TVT PACK SMGH-LF, Model Number: DYNJ41913C;

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: DYNJ57112; b. STANDARD PICC II-LF, Model Number: DYNJSPICC2, PICCNC002; c. SUPERFICAL VENOUS PROCEDURE, Model Number: DYNJ82989; d. SUPERFICIAL VENOUS PROCEDURE, Model Number: DYNJ81267; e. TV IR PICC PACK-LF, Model Number: DYNJ41561D; f. ULTASOUND GUIDED PIV INSERTION, Model Number: IVS3635A; g. ULTRASOUND GUIDED PI

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: DYNJ64862A; b. DBD-C SECTION ADM, Model Number: DYKL1816; c. FETAL SURGERY, Model Number: DYNJ908118A;

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: DYNJ65963A; b. ARTHOGRAM TRAY, Model Number: PAIN1524B; c. ARTHROGRAM TRAY, Model Number: PAIN1524A; d. CARPAL TUNNEL KIT, Model Number: DYNJ63149A; e. CRANIOTOMY CDS, Model Number: CDS981753L; f. CRANIOTOMY CDS-1, Model Number: CDS982889I; g. CRANIOTOMY PACK, Model Number: DYNJ61749A; h. DBD-JOINT INJECTION TRAY,

Medline Industries, LP sits in the heavy federal notice book

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (822 here — heavy-book).

Similar medical devices volume

Nearest multi-notice firms that share this firm's dominant product category.

Frequently Asked Questions

How many federal recall notices name Medline Industries, LP?
PlainRecalls indexes 822 distinct federal recall events naming Medline Industries, LP - Northfield, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Medline Industries, LP sit among other recalling firms?
Medline Industries, LP - Northfield ranks #2 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Medline Industries, LP's notices?
FDA Devices accounts for 812 of this firm's 822 indexed notices across 2 issuing agencies.
What product category dominates Medline Industries, LP's filing book?
Filings for Medline Industries, LP - Northfield span 3 product categories, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous?
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Medline Industries, LP - Northfield: 822 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Medline Industries, LP - Northfield; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026