PlainRecalls

MEDLINE INDUSTRIES, LP - Northfield

532 recalls on record · Latest: Oct 1, 2025

MEDLINE INDUSTRIES, LP - Northfield Recall Insight

MEDLINE INDUSTRIES, LP - Northfield appears on 532 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.634% 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 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 37 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 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Sep 18, 2024 to Oct 30, 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 Moderate Oct 30, 2024

Medline brand medical procedure convenience kits, labeled as: a) LITHOTOMY PACK, REF DYNJ24362C; b) MAJOR GYNE LAPAROSCOPY SHSC, REF DYNJ46774B;…

FDA Devices Moderate Oct 30, 2024

Medline brand medical procedure convenience kits, labeled as: a) PLASTIC PACK, REF DYNJ42735A; b) DR SELEM PACK, REF DYNJ43457; c) BREAST PK T…

FDA Devices Moderate Oct 30, 2024

Medline brand medical procedure convenience kits, labeled as: a) TRAY ADD A CATH FOL UM MF 10ML, REF DYND150200S; b) TRAY FOL LATX UM COUD 16FR …

FDA Devices Moderate Oct 30, 2024

Medline CHEST TUBE INSERTION TRAY ADUL, REF CHT1165; medical procedure convenience kit

FDA Devices Moderate Oct 30, 2024

Medline DENTAL PACK, REF DYNJ64086B; medical procedure convenience kit

FDA Devices Moderate Oct 30, 2024

Medline brand, medical procedure convenience kits, labeled as: a) CUH OPEN HEART A B C - CDS, REF CDS983202I; a) PICC INSERTION KIT, REF DYNDC24…

FDA Devices Moderate Oct 30, 2024

Centurion OB TRAY, REF MNS13965A; medical procedure convenience kit

FDA Devices Moderate Oct 30, 2024

Medline EYE PACK, REF LYN036EPESB; medical procedure convenience kit

FDA Devices Moderate Oct 30, 2024

Medline AMBULATORY MINI PACK, REF DYNJ82579; medical procedure convenience kit

FDA Devices Moderate Oct 30, 2024

Medline brand medical procedure convenience kits, labeled as: 1) NEW LONDON TOTAL KNEE CDS, REF CDS982519W; 2) HAND/FOOT CDS, REF CDS984003A; …

FDA Devices Moderate Oct 30, 2024

Medline brand medical procedure convenience kits, labeled as: 1) EYE PACK, REF DYNJ19492L; 2) PHACO PACK, REF DYNJ22354L; 3) EYE PACK, REF DYNJ24…

FDA Devices Moderate Oct 30, 2024

Medline brand medical procedure convenience kit, labeled as: a) PAIN PROCEDURE PACK, REF DYNJ80370A; b) DR HEFZY BLOCK TRAY, REF DYNJRA1854A

FDA Devices Moderate Oct 30, 2024

Medline DIALYSIS PACK, REF DYNJ36932A; medical procedure convenience kit

FDA Devices Moderate Oct 30, 2024

Centurion EP LAB INSTRUMENT KIT, REF MNS10480; medical procedure convenience kit

FDA Devices Moderate Oct 30, 2024

Medline CENTRAL CATHETER INSERTION TRA, REF CVI680C; medical procedure convenience kit

FDA Devices Moderate Oct 30, 2024

Medline TUBAL LIGATION PACK, REF DYNJ66230B; medical procedure convenience kit

FDA Devices Moderate Oct 30, 2024

Medline brand medical procedure convenience kits, labeled as: 1) THORACENTESIS TRAY, REF 00-400616J; 2) HH PACK SONICATION SPEC CONTAI, REF 3706WHST…

FDA Devices Moderate Oct 30, 2024

Centurion PEDIATRIC/ADULT TRACHEOSTOMY T, REF TC7895; medical procedure convenience kit

FDA Devices Moderate Oct 30, 2024

Medline brand, medical procedure convenience kits, labeled as: a) RADIOLOGY LP TRAY, REF DYNDH1609; b) CARDIAC CATH PACK-LF, REF DYNJ19010I; c…

FDA Devices Moderate Oct 30, 2024

Medline brand medical procedure convenience kits, labeled as: a) UNIVERSAL DRAPE PACK, REF DYNJ44114; b) DRAPE PACK, REF DYNJ82663B

FDA Devices Moderate Oct 30, 2024

(1) Centurion Sterile CirClamp, Reorder #200CR; (2) Centurion CirClamp with 1.1cm Bell and Insert, Reorder #210CR, Sterile; (3) Centurion CirClamp …

FDA Devices Moderate Oct 23, 2024

MEDLINE KIT CV I II, REF DYNJ906071B

FDA Devices Moderate Oct 23, 2024

MEDLINE OPEN HEART, REF DYNJ904261B

FDA Devices Moderate Oct 23, 2024

MEDLINE OPEN HEART PACK, REF DYNJ66216C

FDA Devices Moderate Oct 23, 2024

MEDLINE HEART CABG CDS, REF CDS983376R

FDA Devices Moderate Oct 16, 2024

Medline Sterile Laparoscopy Pack, DYNJ68187A (REF), containing the component ConMed/Unimax Detachable Endo Pocket

FDA Devices Moderate Oct 16, 2024

MEDLINE Automatic Digital Blood Pressure Monitor, REF MDS1001UT.

FDA Devices Moderate Oct 16, 2024

MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001U.

FDA Devices Moderate Oct 16, 2024

MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001

FDA Devices Moderate Sep 25, 2024

Medline Contro-Bulb Syringe, REF DYND20125; bulb irrigation syringe

FDA Devices Moderate Sep 18, 2024

Medline convenience kits containing semi-rigid suction liners labeled as follows: a) AMB VITRECTOMY, Pack Number DYNJ59921B; b) AMB VITRECTOMY, …

FDA Devices Moderate Sep 18, 2024

Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider, Nano-Coated, Compatible w/ FT10 37 cm FT10 SW Version 4.0.1.15 or lower. …

FDA Devices Moderate Sep 18, 2024

Medline ReNewal Reprocessed Covidien LigaSure Blunt Tip, Sealer/Divider, Nano-Coated, Compatible w/ FT10 37cm FT10 SW Version 4.0.1.15 or lower. Item…

FDA Devices Moderate Sep 18, 2024

Medline Convenience kits, labeled as: 1) SUTURING SET PACK ASSY P791011, Pack Number 59112; 2) SUTURE SET, Pack Number DYNDL1984; 3) CLOSING …

FDA Devices Moderate Sep 18, 2024

Medline Convenience kits labeled as: 1) KIT MANIFOLD CSTM-NORTHRIDGE, Pack Number 129736 ; 2) KIT LEFT HEART-VA MED, Pack Number 132701; 3) KI…

FDA Devices Moderate Sep 18, 2024

Medline Convenience kits labeled as: 1) LABOR & DELIVERY CDS, Pack Number CDS830039AD; 2) FETAL SURGERY CDS-LF, Pack Number CDS840214P ; 3) OB PR…

FDA Devices Moderate Sep 18, 2024

Medline Convenience kits labeled as: 1) ADMIT KIT , Pack Number DYKA1225B; 2) BRANSON SUPPLEMENTAL PACK , Pack Number DYNDA3019; 3) L & D PACK…

FDA Devices Moderate Sep 18, 2024

Medline Convenience kits labeled as: 1) CENTRAL LINE CDS, Pack Number CDS930092U ; 2) SMALL WOUND TRAY, Pack Number DYNDA1822; 3) RADIOLOGY UTILI…

FDA Devices Moderate Sep 18, 2024

Medline Convenience kits labeled as: 1) UROLOGY MINOR CDS , Pack Number CDS980371J ; 2) UROLOGY MINOR CDS , Pack Number CDS980371K ; 3) CIRCUM…

FDA Devices Moderate Sep 18, 2024

Medline Convenience kits labeled as: 1) STEREOTACTIC BREAST BIOPSY TRA, Pack Number BT1095 ; 2) BREAST BIOPSY TRAY, Pack Number MNS5070; 3) BR…

FDA Devices Moderate Sep 18, 2024

Medline convenience kits containing semi-rigid suction liners labeled as follows: MTHZ GYN LAPAROSCOPY, Pack Number DYNJ909739

FDA Devices Moderate Sep 18, 2024

Medline Convenience kits labeled as: 1) NHP BREAST BIOPSY PACK, Pack Number DYNJ17400B; 2) BREAST BIOPSY TRAY, Pack Number DYNJ32049A ; 3) BRE…

FDA Devices Moderate Sep 18, 2024

Medline Convenience kits labeled as: 1) CYSTO PACK, Pack Number DYNJ42742D; 2) CYSTO PACK, Pack Number DYNJ42799

FDA Devices Moderate Sep 18, 2024

Medline Convenience kits, labeled as: 1) TRACHEOTOMY TRAY, Pack Number DYNDA1894; 2) TRACHEOSTOMY, Pack Number DYNJ45495G ; 3) TRACH PACK, Pac…

FDA Devices Moderate Sep 18, 2024

Medline Convenience kits labeled as: 1) CVC INSERTION PACK, Pack Number CVI4720A ; 2) CVC INSERTION PACK, Pack Number CVI4720AH; 3) CATHETER I…

FDA Devices Moderate Sep 18, 2024

Medline ReNewal Reprocessed Covidien LigaSure Impact, Sealer/Divider, Nano-Coated, Compatible w/ FT10 18cm FT10 SW Version 4.0.1.15 or lower. Item N…

FDA Devices Moderate Sep 18, 2024

Medline Convenience kits labeled as: 1) EP DRAPE PACK-LF, Pack Number DYNJ0209716K ; 2) MERCY COMBINED PACK-LF, Pack Number DYNJ0233004D ; 3) …

FDA Devices Moderate Sep 18, 2024

Medline convenience kits containing semi-rigid suction liners labeled as follows: a) ANESTHESIA CIRCUIT-LF, Pack Number DYNJAA0311C; b) ANESTHESIA…

FDA Devices Moderate Sep 18, 2024

Medline convenience kits containing semi-rigid suction liners labeled as follows: MERCY TIFFIN C-SECTION, Pack Number DYNJ909732

FDA Devices Moderate Sep 18, 2024

Medline Convenience kits labeled as: 1) OR CLEAN UP KIT, Pack Number DYK1002355X3, 2) CLEANING & CUTTING, Pack Number DYNJ84657

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

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