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 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 49 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 Oct 30, 2024 to Dec 11, 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 Dec 11, 2024

MEDLINE convenience kits labeled as: 2) ABDOMINAL LAPAROSCOPY, REF CDS760057K; 3) ABDOMINAL LAPAROSCOPY, REF CDS760057L; 4) MAJOR LAPAROTOMY CDS,…

FDA Devices Moderate Dec 4, 2024

MEDLINE procedure kits labeled as follows: 1) CONT EPI 20G W/HUSTEAD, REF PAIN1069B; 2) CSE TRAY, REF PAIN1941; 3) TRAY CON EPID 20G NYL W/TUOHY,…

FDA Devices Moderate Dec 4, 2024

MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE, REF EPICATH19 2) 20G EPI CATH SINGLE STERILE, REF EPICATH20

FDA Devices Moderate Dec 4, 2024

(1) Medline Pacer Implant Pack, REF DYNJ59194A, 4 kits/case, sterile; and (2) Medline Thoracotomy Morristown, REF DYNJ904220F, 1 kit/case, non-steri…

FDA Devices Moderate Dec 4, 2024

MEDLINE procedure kits labeled as follows: 1) ECHOSTIM BLOCK SET, REF DYNJRA9043S; 2) ULTRASOUND BLOCK PREP TRAY, REF PAIN1622A

FDA Devices Moderate Dec 4, 2024

(1) Medline Open Heart CDS, REF CDS840132O, packaged 1 kit/case, non-sterile; and (2) Medline Dr. Davies CV, REF DYNJ903016G, packaged 1 kit/case, n…

FDA Devices Moderate Dec 4, 2024

Medline Shoulder Repair Pack-LF, REF DYNJ82607, 2 kits/case, sterile.

FDA Devices Moderate Dec 4, 2024

MEDLINE procedure kits labeled as follows: 1) COMBINED SPINAL AND EPIDURAL, REF DYNJRA1268B; 2) COMBINED SPINAL AND EPIDURAL, REF DYNJRA1268C; …

FDA Devices Moderate Dec 4, 2024

MEDLINE procedure kits labeled as follows: 1) PERIPHERAL CONTINUOUS NERVE BL, REF PAIN1423A; 2) CONT. 20G EPI MRI COMPATIBLE, REF PAIN1470A; 3) E…

FDA Devices Moderate Dec 4, 2024

MEDLINE procedure kits labeled as follows: 1) L&D CONTINUOUS EPIDURAL TRAY, REF PAIN1699; 2) L&D CONTINUOUS EPIDURAL TRAY, REF PAIN1699A

FDA Devices Moderate Dec 4, 2024

ENDO KIT, Medline Kit SKU DYKE1577A, Component Number 57469, 10 per case; Medline Convenience Kits containing Single Use Biopsy Valve MAJ-1555

FDA Devices Moderate Dec 4, 2024

MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT, REF PAIN1876A

FDA Devices Moderate Dec 4, 2024

MEDLINE NEXUS 19/20G CATH CONNECTOR, Medline SKU REF NEXCONNECT, Catheter Connector

FDA Devices Moderate Nov 20, 2024

Lab Kit, SKU DYLAB1018; Component No. 503581

FDA Devices Moderate Nov 20, 2024

URINE COLLECTION VHC, SKU DYLAB1016; Component No. 503581

FDA Devices Moderate Nov 20, 2024

Clean Catch Kit, SKU DYKM1833A; Component No. 503581

FDA Devices Moderate Nov 20, 2024

CARROLLTON HIP FX Convenience kit used for surgical procedures, SKU SYNJ910003A

FDA Devices Moderate Nov 20, 2024

UA KIT, SKU DYKM1690A; Component No. 503581

FDA Devices Moderate Nov 20, 2024

URINE COLLECTION KIT, SKU DYKM1848A DYKM2005 DYKM2151 DYLAB1004 DYLAB1004A DYLAB1006 DYLAB1012 ; Component No. 503581

FDA Devices Moderate Nov 20, 2024

Medline Iris Scissors, Single-Use, Curved, Standard 4.5 , Model Nos. DYNJ04049 (cases), DYNJ04049H (eaches)

FDA Devices Moderate Nov 20, 2024

ARTHROSCOPY Convenience kit used for surgical procedures, SKU SYNJ910004C

FDA Devices Moderate Nov 20, 2024

URINE KIT, SKU DYKM1845; Component No. 503581

FDA Devices Moderate Nov 20, 2024

URINE KIT W/BD CUP, SKU DYLAB1001A; Component No. 503581

FDA Devices Moderate Nov 20, 2024

URINALYSIS KIT 4, SKU DYLAB1021; Component No. 503581

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 30, 2024

Medline IV TEAM PICC, REF DYNJ48222; medical procedure convenience kit

FDA Devices Moderate Oct 30, 2024

Medline brand medical procedure convenience kits, labeled as: a) ABDOMINAL HYSTERECTOMY TEGH-LF, REF DYNJ46730; b) HYSTEROSCOPY PACK, REF DYNJ49…

FDA Devices Moderate Oct 30, 2024

Medline brand medical procedure convenience kits, labeled as: 1) L&D/OB PACK-LF, REF DYNJ0213264O; 2) VAG DELIVERY HLTH ALLIA PK-LF, REF DYNJ03754…

FDA Devices Moderate Oct 30, 2024

Medline brand medical procedure convenience kits, labeled as: 1) CYSTO CDS, REF CDS983525D; 2) CYSTO CDS, REF CDS983525D; 3) CYSTO PACK-LF, RE…

FDA Devices Moderate Oct 30, 2024

Medline brand, medical procedure convenience kits, labeled as: a) SET UP PACK, REF DYNJ36320A; b) ANGIOGRAM WRO-LF, REF DYNJ41876B

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.