Manufacturer

MEDLINE INDUSTRIES, LP - Northfield

787 recalls in our database name MEDLINE INDUSTRIES, LP - Northfield as the manufacturing or recalling firm.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

51–75 of 787

HighFDA (Devices)·Z-1611-2025·2025-04-23
Medline Sterile Obstetrical Procedure Kits Recalled for Potential Packaging Seal Defects
Medline is recalling 21,935 sterile convenience kits used for obstetrical procedures due to potential open or weak seals on breather pouches that could compromise product sterility. The kits were distributed nationwide and internationally.
Product
Medline Convenience kits used for various procedures: 1) LABOR AND DELIVERY PACK-LF, Model Number: DYNJ26971L; 2) VAGINAL DELIVERY PACK-LF, Model Number: DYNJ0378319P; 3) VUWC OB PACK, Model Number: DYNJ64017B; 4) OB PROTECTION PACK NO GAUZE, Model Number: DYNJHTLD04A; 5
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1599-2025·2025-04-23
Medline Convenience Kits Recalled for Potential Packaging Seal Defect
Medline has recalled two models of convenience kits due to potential open or weak seals on packaging breather pouches. Approximately 530 units distributed worldwide may be affected.
Product
Medline Convenience kits used for various procedures: 1) T&A ENDO PACK, Model Number: DYNJ59620A; 2) TRAY ADD A CATH FOL UM MF 10ML, Model Number: DYND150200S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1586-2025·2025-04-23
Medline Convenience Kits Recalled Due to Weak Packaging Seals
Medline is recalling Convenience kits due to open or weak seals on breather pouches used in sterile packaging. The recalled lot 24KBI045 was distributed nationwide and internationally.
Product
Medline Convenience kits used for various procedures: 1) INTUBATION TRAY, Model Number: MNS10395;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1608-2025·2025-04-23
Medline Universal Drape Pack Medical Kits Recalled for Weak Sterile Seals
Medline is recalling Universal Drape Pack convenience kits due to potential open or weak seals on sterile packaging pouches. Weak seals may compromise product sterility.
Product
Medline Convenience kits used for various procedures: 1) UNIVERSAL DRAPE PACK, Model Number: DYNJCD0239
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1606-2025·2025-04-23
Medline Skin Lesion Convenience Kits Recalled for Compromised Packaging Seals
Medline Industries is recalling Skin Lesion convenience kits (Model MNS6270, Lot 24KBD496) due to potential open or weak seals on breather pouches. The defective seals may compromise the integrity of the sterile medical kits.
Product
Medline Convenience kits used for various procedures: 1) SKIN LESION SET, Model Number: MNS6270
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1596-2025·2025-04-23
Medline Rhinoplasty Kits Recalled for Weak Packaging Seals
Medline is recalling 56 Rhinoplasty Packs due to weak or open seals on breather pouches. The packaging defect may compromise sterility of the surgical kits.
Product
Medline Convenience kits used for various procedures: 1) RHINOPLASTY PACK, Model Number: DYNJ27333F
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1591-2025·2025-04-23
Medline Sterile Convenience Kits Recalled Due to Weak Breather Pouch Seals
Medline is recalling 4,022 sterile procedure kits due to potential open or weak seals on breather pouches that could compromise sterility.
Product
Medline Convenience kits used for various procedures: 1) ANGIOGRAPHY DRAPE PACK, Model Number: HCP075G; 2) ENSEMBLE CORONAROGRAPHIE-LF, Model Number: DYNJ64354A; 3) RADIOL ANGIO PACK-LF, Model Number: 0M-CP01029D; 4) ARTERIOGRAM PACK 2, Model Number: DYNJ81454B; 5) CATH
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1590-2025·2025-04-23
Medline Sterile Procedure Kits Recalled Due to Weak Breather Pouch Seals
Medline is recalling sterile convenience kits used for various procedures because breather pouches may have open or weak seals, which could compromise sterility during storage or transport.
Product
Medline Convenience kits used for various procedures: 1) ANGIO CONSOLIDATED PACK, Model Number: DYNJHTCAD1; 2) ANGIOGRAPHY TRAY-LF, Model Number: DYNJ05350V; 3) ANGIOGRAPHY PACK, Model Number: DYNJ38144C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1613-2025·2025-04-23
Medline Sterile Surgical Kits: Weak Packaging Seals on Breather Pouches
Medline is recalling 706 units of sterile surgical convenience kits due to potential open or weak seals on packaging breather pouches that could compromise product sterility.
Product
Medline Convenience kits used for various procedures: 1) STANDARD D&C, Model Number: DYNJ69733; 2) NHS - LAP BOWEL GNG, Model Number: DYNJ39904A; 3) LAPAROSCOPY GYN SURGERY PA, Model Number: DYNJ64651A; 4) GYNE - LITHOTOMY MAJOR-LF, Model Number: DYNJ49250F; 5) ENS. GYNE
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1595-2025·2025-04-23
Medline Dental Convenience Kits Recalled for Weak Breather Pouch Seals
Medline Industries is recalling select sterile dental convenience kits due to potential open or weak seals on breather pouches. The compromised seals could allow contamination of sterile products.
Product
Medline Convenience kits used for various procedures: 1) DENTAL PACK-LF, Model Number: DYNJ84880; 2) DENTAL PACK, Model Number: DYNJ56229A; 3) DENTAL PACK-LF, Model Number: PHS807626F; 4) DENTAL PACK SMGH, Model Number: DYNJ41929D; 5) DENTAL PACK, Model Number: DYNJ51841
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1612-2025·2025-04-23
Medline Sterile Convenience Kits Recalled for Potential Breather Pouch Seal Defects
Medline is recalling certain sterile convenience kits due to potential open or weak seals on breather pouches used for packaging. Compromised seals could allow contamination and compromise the sterility of the kits.
Product
Medline Convenience kits used for various procedures: 1) CW PERI GYN, Model Number: DYNJ80807B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1618-2025·2025-04-23
Select Sterile Convenience Kits Recalled Due to Weak Breather Pouch Seals
Medline Industries is recalling select sterile convenience kits due to potential open or weak seals on breather pouches. The affected packaging could compromise sterility.
Product
Refer to RES
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1601-2025·2025-04-23
Medline convenience kits recalled due to weak packaging seals
Medline Industries is recalling 116 sterile convenience kits with Model Number DYNJ907733B due to potential weak seals on breather pouches. Compromised seals may affect product sterility during storage and distribution.
Product
Medline Convenience kits used for various procedures: 1) MINOR BASIN -SMH, Model Number: DYNJ907733B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1594-2025·2025-04-23
Medline Convenience Kits Recalled for Potentially Weak Sterile Seals
Medline Industries is recalling 1126 Convenience kits used for various medical procedures due to potential open or weak seals on breather pouches. Compromised seals may allow contaminants to reach sterile contents, though no illnesses or injuries have been reported.
Product
Medline Convenience kits used for various procedures: 1) LARGE BIOPSY PACK NTX, Model Number: DYNJ68393A; 2) SOFT TISSUE BIOPSY PACK, Model Number: DYNJ81441B; 3) BILAT TESTICULAR SPERM EXTRACT, Model Number: DYNJ68303; 4) PROCEDURE MINEURE BJC-LF, Model Number: DYNJ41678B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1609-2025·2025-04-23
Medline hernia repair kits recalled for weak packaging seals
Medline is recalling hernia repair kits due to potential open or weak seals on packaging pouches. The defect could compromise product sterility.
Product
Medline Convenience kits used for various procedures: 1) HERNIA REPAIR TOTE, Model Number: DYNJ908337C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1619-2025·2025-04-23
Medline Arthroscopy Convenience Kits Recalled for Weak Packaging Seals
Medline Industries recalled 222 arthroscopy convenience kits due to potential open or weak seals on breather pouches used for sterile packaging. The compromised seals could affect the ability to maintain sterility of the surgical instruments.
Product
Medline Convenience kits used for various procedures: 1) ARTHROSCOPIE DU GENOU-LF, Model Number: DYNJ40229A; 2) ARTHROSCOPY PACK-LF, Model Number: OPK382N; 3) ARTHROSCOPY NEW TEGH-LF, Model Number: DYNJ46723B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1593-2025·2025-04-23
Medline sterile medical procedure kits recalled for seal failure risk
Medline is recalling approximately 3,808 sterile medical procedure kits due to potential open or weak seals on breather pouches. Broken seals could expose the devices to contamination.
Product
Medline Convenience kits used for various procedures: 1) LINE INSERTION PACK, Model Number: DYNJ44949C; 2) PICC LINE INSERTION BJC-LF, Model Number: DYNJ41682C; 3) SUPERFICIAL VENOUS PROCEDURE, Model Number: DYNJ81267A; 4) ILR INSERTION-REMOVAL PACK, Model Number: DYNJ8243
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1587-2025·2025-04-23
Medline Rhinoplasty Convenience Kit Recalled Due to Potential Seal Failures
Medline is recalling Rhinoplasty Convenience Kits (Model DYNJ84116A, Lot 24IBH580) due to potential open or weak seals on breather pouches. Compromised seals could affect package sterility, though no illnesses have been reported.
Product
Medline Convenience kits used for various procedures: 1) RHINOPLASTY PACK, Model Number: DYNJ84116A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1588-2025·2025-04-23
Medline Sterile Convenience Kits Recalled for Weak Breather Pouch Seals
Medline is recalling PAIN PACK and PAIN TRIAL PACK sterile convenience kits due to potential open or weak seals on breather pouches, which could compromise product sterility.
Product
Medline Convenience kits used for various procedures: 1) PAIN PACK, Model Number: DYNJ67577A; 2) PAIN TRIAL PACK, Model Number: DYNJ67576A;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1610-2025·2025-04-23
Medline sterile convenience kits recalled for weak breather pouch seals
Medline is recalling sterile convenience kits due to weak or open seals on breather pouches used for packaging. Compromised seals could allow contamination of sterile medical devices.
Product
Medline Convenience kits used for various procedures: 1) NEURO PACK WRO-LF, Model Number: DYNJ41856C; 2) STIM IMPLANT PACK, Model Number: DYNJ53032C; 3) WMC VP SHUNT PACK-LF, Model Number: DYNJ50629M; 4) SHUNT PACK, Model Number: DYNJ40040C; 5) STIM IMPLANT PACK, Model N
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1459-2025·2025-04-16
Medline medical procedure kits recalled for aortic cannula connector defect
Medline is recalling 1,247 medical procedure kits containing Medtronic Aortic Root Cannula due to excess material in male connectors. The defect poses risks during cardiac procedures and affects kits distributed across nine U.S. states.
Product
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CPB ADJUNCT PACK, DR. C PACK, PK CUST CV A&B C CO, TOL DR R PACK, TOL DR. C PACK, TOL DR. M PACK.
Category
Medical Device
Distribution
9 states
SevereFDA (Devices)·Z-1457-2025·2025-04-16
Medline medical procedure kits recalled for defective aortic cannula connectors
Medline is recalling 468 medical procedure kits containing Medtronic Aortic Root Cannulas due to excess material in the male connectors that could affect proper assembly during cardiac procedures.
Product
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: TOL DR R PACK
Category
Medical Device
Distribution
9 states
SevereFDA (Devices)·Z-1456-2025·2025-04-16
Medline Medical Procedure Kits With Aortic Cannula Recalled
Medline is recalling 1310 medical procedure kits containing Medtronic Aortic Root Cannula distributed across nine U.S. states. The FDA classified this as a Class I recall.
Product
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CABG OPNHRT S HSP, CARDIAC CABG, CARDIAC PACK, DR D AC PACK, HEART BASIN PACK-LF, K OH COMPONENT PACK, OPEN HEART ADULT PART 1 CDS, OPEN HEART B PACK-LF, OPEN HEART PACK, Z OPEN HEART
Category
Medical Device
Distribution
9 states
SevereFDA (Devices)·Z-1458-2025·2025-04-16
Medical procedure kits recalled for aortic cannula assembly defect
Medline procedure kits with Medtronic aortic root cannulas are recalled for potential excess material in the male lures, affecting 320 units distributed in eight US states.
Product
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: HEART BASIN PACK-LF
Category
Medical Device
Distribution
9 states
SevereFDA (Devices)·Z-1505-2025·2025-04-16
Medline medical kits recalled due to defective endotracheal tubes
Medline Industries is recalling approximately 1,550 medical convenience kits containing defective endotracheal tubes manufactured by Smiths Medical. The affected kits include neonatal and pediatric intubation and resuscitation equipment distributed in California.
Product
Medline medical convenience kits labeled as: 1) NEONATAL INTUBATION TRAY, REF ACC010371C; 2) NEWBORN RESUSCITATION KIT, REF ACC010381A; 3) NEWBORN RESUSCITATION KIT, REF ACC010381B; 4) NEWBORN RESUSCITATION KIT, REF ACC010381C; 5) PEDS GREY-PINK-RED, REF ACC010395; 6
Category
Medical Device
Distribution
0 states