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 4 critical, 46 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 48 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 Apr 10, 2024 to Aug 28, 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 Aug 28, 2024

Medline medical procedure kits labeled as follows: a) ARTHROSCOPY, REF DYNJ909699; b) BACK CDS, REF CDS984000C; c) EXTREMITY, REF DYNJ900847A;…

FDA Devices Critical Aug 14, 2024

Medline procedure kits labeled as: 1) NEPHROLOGY PACK, Pack Number DYNJ59089; 2) NERVE BLOCK TRAY, Pack Number DYNJRA1221A

FDA Devices Moderate Aug 14, 2024

Centurion procedure kits labeled as: 1) CVC INSERT BUNDLE 16CM, Pack Number ECVC3260; 2) CVC DOUBLE LUMEN 16CM, Pack Number ECVC8105

FDA Devices Moderate Aug 14, 2024

Centurion procedure kits labeled as NEURO ANGIO PACK, Pack Number DYNDA1431A

FDA Devices Critical Aug 14, 2024

Medline procedure kits labeled as: 1) WMC HYBRID OR PACK PART 1 , Pack Number CMPJ08068F ; 2) VASCULAR PACK , Pack Number CMPJ11455B ; 3) SALE…

FDA Devices Critical Aug 14, 2024

Medline procedure kits labeled as: 1) CONTINUOUS BLOCK, Pack Number DYNJRA0960C; 2) COMBINED SPINAL AND EPIDURAL, Pack Number DYNJRA1268C; 3) …

FDA Devices Moderate Jul 10, 2024

Sterile convenience kits: a. Medline Retrograde PK-22025203-LF, Pack #DYNJ47873K, containing a Pure Pouch containing component Sterile Curved Kel…

FDA Devices Moderate Jul 10, 2024

Non-sterile convenience kits: a. Medline Difficult Airway Tray W/O Cook, Pack #ACC010578, containing a Pure Pouch with component Reorder #DYNJ040…

FDA Devices Moderate Jul 10, 2024

Sterile surgical convenience kit: Medline Neuro IR Pack, Pack #DYNJ56073C, containing a Pure Pouch with component Medline Reorder #DYNJ04048, Kel…

FDA Devices Moderate Jul 10, 2024

Non-sterile convenience kits: a. Medline CC Drawer 4 IV Circulation, Pack #ACC010254B, containing a Pure Pouch component DYND04000, O.R. Scissors …

FDA Devices Moderate Jul 10, 2024

Non-sterile convenience kits: Medline Open Heart CDS, Pack #CDS981759C, containing a Pure Pouch with component Reorder #DYNJ04048, Kelly Forceps/S…

FDA Devices Moderate Jul 10, 2024

Sterile surgical convenience kits: a. Medline Cath Lab Special Procedure, Pack #00-RDF0360, containing a Pure Pouch with component Medline Reord…

FDA Devices Moderate Jul 10, 2024

Nonsterile convenience kits: a. Medline Delivery, Pack #DYNJ901130I, containing a Pure Pouch with component Reorder #DYND04000, O.R. Scissors, S/…

FDA Devices Moderate Jul 10, 2024

Sterile convenience kit: Medline Birthing Room Pack, Pack #DYNJ38429D, containing a Pure Pouch component Sterile Sharp/Blunt Scissors 5.5", Reorde…

FDA Devices Moderate Jul 10, 2024

Sterile surgical convenience kit: Medline Retrograde PK-22025203-LF, Pack #DYNJ47873L, containing a Pure Pouch with component Sterile Curved Kelly…

FDA Devices Moderate Jun 12, 2024

MEDLINE LUER SLIP DISPOSABLE SYRINGE WITHOUT NEEDLE, REF SYR101020

FDA Devices Moderate Jun 12, 2024

MEDLINE LUER LOCK DISPOSABLE SYRINGE WITHOUT NEEDLE, REF SYR101010

FDA Devices Moderate Jun 12, 2024

Syringes labeled as: a) SYR 10ML L/L CONTROL, Item Numbers: 1. DNSC91881, 2. DYNJSYRPPC10; b) SYRINGE 20ML BLUE L/L LOW PR, Item Number: DYN…

FDA Devices Moderate Jun 12, 2024

MEDLINE STERILE IRIS SCISSORS CVD/STD REF DYNJ04049 (case) and DYNJ04049H (individual unit)

FDA Devices Critical Jun 5, 2024

Medline Sub-G Endotracheal Tube with Subglottic Suctioning: (1) REF DYNJ18860, Polyurethane Cuff 6.0 mm ID; (2) REF DYNJ18865, Polyurethane Cuff …

FDA Devices Moderate Jun 5, 2024

Medline medical procedure kits, labeled as follows: a) PARACERVICAL PUD TRAY, REF DYNDH1832; b) AHS PARACERVICAL/PUDENDAL KIT, REF DYNJRA2210; …

FDA Devices Moderate Jun 5, 2024

Centurion OB INSTRUMENT TRAY, REF MN3925; Medical procedure convenience tray

FDA Devices Moderate May 22, 2024

Namic FLUID DELIVERY SET, REF 91300040

FDA Devices Moderate May 22, 2024

namic CONVENIENCE KIT, a) CAROTID MANIFOLD KIT, REF 60011045; b) 3V MANIFOLD KIT ON WITH NAMIC DT & WASTE MANAGEMENT, REF 60070582; c) LEFT HEA…

FDA Devices Moderate Apr 17, 2024

Bed Assist Bars, labeled as follows: a) Medline, Model Number BA6800, b) Medline Martha Stewart, Model Number MDS6800BAMMS

FDA Devices Moderate Apr 17, 2024

Bed Assist Bars, labeled as follows: a) Medline SwivAssist Bar, Model Number MDS6800SWIV (case of 3), b) Medline SwivAssist Bar, Model Number MD…

FDA Devices Moderate Apr 10, 2024

Centurion manual surgical kits labeled as: a) STERILE 4-1/2" S/S SCISSOR (SS5031), Product Code 65145; b) STERILE S/B SCISSOR 4-1/2" (I142), Prod…

FDA Devices Moderate Apr 10, 2024

Centurion DISP.UMBILICAL CORD CLAMP CUTTER(CTR300), Product Code 67335

FDA Devices Moderate Apr 10, 2024

Centurion STERILE COTTON DENTAL ROLLS 6/PK, Product Code 9125ST6

FDA Devices Moderate Apr 10, 2024

Centurion Hemostat kits labeled as: a) STERILE CURV KELLY HEMOSTAT, Product Code 65340; b) STERILE CURV MOSQUITO HEMOSTAT (MHS103), Product Code …

FDA Devices Moderate Apr 10, 2024

MEDLINE SWABSTICKS PVP 3 PK, Product Code DYNDA2724

FDA Devices Moderate Apr 10, 2024

MEDLINE M1S0179 STRL TAPE/PEN PACK, Product Code P519582A

FDA Devices Moderate Apr 10, 2024

Centurion STERILE #16 RUBBER BAND, Product Code EB16

FDA Devices Moderate Apr 10, 2024

Centurion retractor kits labeled as: a) STERILE 6-1/2" SENN RETRACTOR (ST7185), Product Code 66795; b) STERILE RAGNELL RETRACTOR (RR602), Product …

FDA Devices Moderate Apr 10, 2024

Centurion Clamp kits labeled as: a) STERILE BACKHAUS TOWEL CLAMP (BTC173), Product Code 66520; b) STERILE TOWEL CLAMP, Product Code A547ST; c) …

FDA Devices Moderate Apr 10, 2024

MEDLINE SWABSTICKS ALCOHOL 3PK, Product code DYNDA2723

FDA Devices Moderate Apr 10, 2024

Centurion manual surgical kits labeled as: a) STERILE ALLIS TISS FCP 10", Product Code I68905; b) VAGINAL REPAIR KIT, Product Code MNS11505; c)…

FDA Devices Moderate Apr 10, 2024

Centurion hook kits labeled as: a) STERILE SKIN HOOK FINE (EA3975F), Product Code 66660; b) STERILE SMALL 2 PRONG SKIN HOOK (25754), Product Code …

FDA Devices Moderate Apr 10, 2024

Centurion STERILE #5 LARYNGEAL MIRROR(505709), Product Code 67830

FDA Devices Moderate Apr 10, 2024

Centurion STERILE BLOOD COLLECTION TUBE,10ML, Product Code 6430ST

FDA Devices Moderate Apr 10, 2024

Blood Pressure Unit, Model (REF) Numbers: a) MDS4001, b) MDS4001LA, c) MDS4001PLUS

FDA Devices Moderate Apr 10, 2024

Centurion FCP MAGILL CATH 7.5 IN PED (67575), Product Code 67575

FDA Devices Moderate Apr 10, 2024

Centurion Forcep kits labeled as: a) STERILE F/P SPLINTER FORCEP (SF6141), Product Code 66165; b) STERILE WEBSTER NEEDLEHOLDER, Product Code 66185;…

FDA Devices Moderate Apr 10, 2024

MEDLINE 4.5 IN WIRE CUT SCISSORS, Product Code DYND04006

FDA Devices Moderate Apr 10, 2024

Centurion PICC LINE SECUREMENT KIT, Product Code IVS565

FDA Devices Moderate Apr 10, 2024

Centurion STERILE TRACH BRUSH, Product Code 6225ST

FDA Devices Moderate Apr 10, 2024

Centurion kits: a) DENTAL INSTRUMENT KIT, Product Code DH760; b) STERILE COTTON DENTAL ROLLS 6/PK, Product Code 9125ST6; c) DENTAL INSTRUMENT KI…

FDA Devices Moderate Apr 10, 2024

Centurion Manual surgical kits labeled as: a) STERILE S/B WIRE SCISSOR, Product Code 65140; b) SHARP/SHARP SCISSORS 41/2", Product Code 65840; …

FDA Devices Moderate Apr 10, 2024

Centurion manual surgical kits labeled as: a) STERILE TUBE OCCLUDING FORCEP (TO8256), Product Code 66225; b) ST. KELLY HEMO W/TIPS (SK8039), Prod…

FDA Devices Moderate Apr 10, 2024

Centurion STERILE ROUND EAR SPECULUM SET (3, 4, 5), Product Code I68505

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.