Manufacturer

Medline Industries, LP

351 recalls in our database name Medline Industries, LP 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.

176–200 of 351

HighFDA (Devices)·Z-1465-2026·2026-03-04
Dialysis Maintenance Kits Recalled for Defective Silicone Connector Seals
Dialysis kits from Medline and Centurion may have defective silicone seals on connectors that can block fluid flow, interrupt therapy, or allow air and contaminants into the body.
Product
Convenience kits used for dialysis maintenance Medline ADD A CATH DIALYSIS KIT SKU ECVC8415A Centurion CENTRAL LINE INSERTION TRAY SKU DT19810 Centurion DIALYSIS BUNDLE WITH NO CATHETTER SKU CVI4310A Medline DIALYSIS CAP CHANGE KIT SKU DYNDC2425 Medline DIALYSI
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1464-2026·2026-03-04
Medline Dialysis Kit Connectors Recalled for Silicone Seal Defects
Medline Industries recalls dialysis on/off kits with defective silicone seals that may prevent fluid injection/withdrawal and cause therapy delays. Affected units may leak, interrupt therapy, or expose patients to contaminants and air.
Product
Medline Kits containing Tego Connectors Medline DIALYSIS ON/OFF KIT SKU EBSI1746
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1432-2026·2026-03-04
Medline Nail Kit Recalled for Sterile Wound Wash Sterility Deficiency
Medline is recalling 1,640 Nail Kits containing sterile saline wound wash because the manufacturer may not have met minimum sterility assurance levels. The affected kits were distributed nationwide and internationally.
Product
Medline Convenience Kits: 1) NAIL KIT, Model Number: POD14214
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1435-2026·2026-03-04
Meijer Saline Wound Wash Recalled Due to Sterility Assurance Level Failure
Medline Industries is recalling Meijer STERILE saline wound wash because the manufacturer may not have met required sterility standards. The recalled product was distributed nationwide in the US and internationally.
Product
Meijer STERILE saline wound wash, First Aid Cleansing Spray, 0.9% USP SODIUM CHLORIDE, 7.1FL OZ (210 mL), DBD-CAN,SPRAY,7.1-OZ,SALINE,WOUND WASH,S, Model Number MJSALINE7
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1467-2026·2026-03-04
Medline Dialysis Dressing Change Kits Recalled for Defective Tego Connectors
Medline Industries is recalling approximately 31,848 dialysis dressing change kits with defective Tego Connectors. Silicone seals may crack or dome, potentially blocking fluid flow, causing therapy delays, or allowing biological contamination.
Product
Convenience kits containing Tego Connectors: Medline DIALYSIS DRESSING CHANGE SKU EBSI1498 Medline DIALYSIS DRESSING CHANGE KIT SKU EBSI1107 EBSI1596 EBSI1781 EBSI1812 Centurion DIALYSIS/PHERESUS CVC DRSG CHANGE KIT SKU DT22630 Medline DIALYSIS/PHERESIS DRESSING
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1463-2026·2026-03-04
Medline Dialysis Kits Recalled for Defective Silicone Seals
Medline is recalling 516 dialysis insertion kits due to silicone seal defects that may block fluid flow or cause therapy delays. Affected units risk allowing biological contamination or air to enter the body.
Product
Medline Kits containing Tego Connectors: Medline IR Pack, SKU DYNJ67205C Medline NO CATHETER DIALYSIS INSERTION, SKU CVI5200
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1434-2026·2026-03-04
Medline Nail Kit Recalled for Sterile Saline Wound Wash Sterility Failure
Medline has recalled certain Nail Kits because the sterile saline wound wash component may not meet required sterility standards. The affected kits were distributed nationwide and internationally.
Product
Medline Convenience Kits: 1) NAIL KIT, Model Number: DYKM1528
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1433-2026·2026-03-04
Medline Sterile Saline Wound Wash Kits Recalled for Inadequate Sterility
Medline Industries recalls multiple sterile saline wound wash kits due to potential inadequate sterility from manufacturing defects. The affected kits may not meet required sterility standards.
Product
Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION, Model Number: DYKM1361A; 2) TRUNK KIT 1EA, Model Number: DYKM2013; 3) TRUNK KIT 1EA, Model Number: DYKM2013A; 4) RN TRUNK KIT, Model Number: DYKM2699; 5) TRUNK KIT, Model Number: DYKTRUNK1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1420-2026·2026-02-25
Medline surgical and ophthalmology kits recalled for sterilization equipment calibration issues
Medline is recalling 4,853 surgical and ophthalmology convenience kits due to calibration issues with sterilization equipment that could compromise sterility assurance. No illnesses have been reported.
Product
Medline Convenience Kits: 1) KIT OPHTHALMIC RUPTURE GLOBE, Model Number: DYKMBNDL104; 2) KIT OPHTHALMIC RUPTURE GLOBE, Model Number: DYKMBNDL104A; 3) KIT OPHTHALMOLOGY CORNEAL TRAN, Model Number: DYKMBNDL159; 4) KIT OPHTHALMOLOGY CATARACT, Model Number: DYKMBNDL180; 5) K
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1421-2026·2026-02-25
Medline Surgical Kits Recalled Due to Sterilization Equipment Calibration Issues
Medline is recalling surgical convenience kits used in orthopedic procedures due to sterilization equipment calibration issues that could compromise sterility assurance. The recall affects approximately 117,907 units distributed nationwide.
Product
Medline Convenience Kits: 1) SPINAL CDS, Model Number: CDS940087AG; 2) SPINAL CDS, Model Number: CDS940087AI; 3) TOTAL HIP CDS-LF, Model Number: CDS980832Q; 4) TOTAL HIP CDS-LF, Model Number: CDS980832R; 5) TOTAL HIP CDS-LF, Model Number: CDS980832S; 6) TOTAL KNEE CDS-
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1406-2026·2026-02-25
Medline Surgical Drape Pack Recall Due to Sterilization Equipment Calibration Issues
Medline is recalling surgical drape packs due to sterilization equipment calibration issues that could compromise sterility levels. No illnesses have been reported.
Product
Medline Convenience Kits: 1) DRAPE PACK-CHOICE, Model Number: DYNJ63118A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1386-2026·2026-02-25
Medline convenience kits recalled for sterilization equipment calibration issues
Medline is recalling 779 units of five convenience kit models due to calibration issues in sterilization equipment. These issues may compromise the sterility assurance of affected devices.
Product
Medline Convenience Kits: 1) SCC RF PAIN MGMT, Model Number: DYNJ56436A; 2) SCC RF PAIN MGMT, Model Number: DYNJ56436B; 3) CPNB SETUP TRAY, Model Number: DYNJRA1979; 4) CPNB SETUP TRAY, Model Number: DYNJRA1979A; 5) CPNB SETUP TRAY, Model Number: SAMPA0108
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1409-2026·2026-02-25
Medline Convenience Kits Recalled Due to Sterilization Equipment Calibration Issues
Medline is recalling two medical device convenience kits due to calibration issues with sterilization equipment that could impact product sterility.
Product
Medline Convenience Kits: 1) DRAPE PACK, Model Number: DYNJ35363A; 2) SICK KIDS-GENERAL CUSTOM SPLIT, Model Number: SPTPCD10005
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1366-2026·2026-02-25
Medline IV Administration and Extension Sets: Connector Defect Risk
Medline Industries is recalling 926,227 units of IV Administration and Extension Sets due to potential male luer connector defects that may leak, crack, or break during use, risking treatment delays, infection, blood loss, or air embolism.
Product
Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN SET,60DRP,1NEEDLE-FREE VALV, Model Number: DYNDTB0529; 2) IV ADMIN SET, 10DRP, 1NF, 92, Model Number: DYNDTB1029; 3) DBD-IVEXTSET2.4ML2 NEEDLE-FREEVLVE,35, Model Number: DYNDTB1516; 4) DBD-IV ADMIN SE
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1405-2026·2026-02-25
Medline Convenience Kits Recalled Due to Sterilization Equipment Calibration Issues
Medline is recalling 108 Convenience Kits nationwide due to sterilization equipment calibration defects that could compromise sterility assurance on medical closure devices.
Product
Medline Convenience Kits: 1) KIT GENERAL CLOSURE, Model Number: DYKMBNDL200A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1410-2026·2026-02-25
Medline Admission Kits Recalled Due to Sterilization Equipment Calibration Issues
Medline is recalling Admission Kits (Model DYKA1343A) due to calibration problems in sterilization equipment that could compromise the sterility of the devices. The recall affects 1,070 units distributed nationwide.
Product
Medline Convenience Kits: 1) ADMIT KIT, Model Number: DYKA1343A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1397-2026·2026-02-25
Medline surgical kits recalled for potential sterility compromise due to calibration issues
Medline is recalling 4,757 surgical kits and packs due to calibration issues with sterilization equipment that could affect sterility assurance. No illnesses or injuries have been reported.
Product
Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS, Model Number: ACC010499; 2) KIT UROLOGY URETHROPLASTY, Model Number: DYKMBNDL117C; 3) KIT PLASTIC INSERT TISSUE EXPA, Model Number: DYKMBNDL158; 4) KIT PLASTIC ABDOMINOPLASTY, Model Number: DYKMBNDL170; 5) KIT PLASTIC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1395-2026·2026-02-25
Medline Surgical Convenience Kits Recalled Due to Sterilization Calibration Issues
Medline is recalling 82,597 surgical device kits nationwide due to equipment calibration issues that could affect sterilization quality. The kits were used in various surgical procedures.
Product
Medline Convenience Kits: 1) MAJOR LAPAROTOMY CDS, Model Number: CDS860015U; 2) MAJOR LAPAROTOMY CDS, Model Number: CDS860015V; 3) MAJOR LAPAROTOMY CDS, Model Number: CDS860015W; 4) MAJOR LAPAROTOMY CDS, Model Number: CDS860015X; 5) MINOR LAPAROTOMY CDS, Model Number: CD
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1394-2026·2026-02-25
Medline Surgical Device Kits Recalled for Sterilization Equipment Calibration Issues
Medline Industries, LP is recalling 9,051 surgical device kits due to sterilization equipment calibration issues that could compromise sterility assurance levels. The recalled kits may not be adequately sterile despite undergoing validated sterilization processes.
Product
Medline Convenience Kits: 1) CHP COCHLEAR SUPPLEMENT CDS, Model Number: CDS983069G; 2) CHP COCHLEAR SUPPLEMENT CDS, Model Number: CDS983069I; 3) HEAD & NECK CDS-LF, Model Number: CDS983782C; 4) BAPTIST FLOYD BRONCHOSCOPY, Model Number: DYKE1456D; 5) BRONCHOSCOPY SETUP KI
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1385-2026·2026-02-25
Medline tracheostomy kits recalled for sterilization equipment calibration issues
Medline is recalling 753 tracheostomy convenience kits due to calibration issues in sterilization equipment that could affect sterility assurance level.
Product
Medline Convenience Kits: 1) KIT STC TRACHEOSTOMY, Model Number: DYKMBNDL55; 2) KIT STC TRACHEOSTOMY, Model Number: DYKMBNDL55A; 3) TRACH TOTE, Model Number: DYNJ85691
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1398-2026·2026-02-25
Medline Lithotomy Packs Recalled for Sterilization Equipment Calibration Issues
Medline has recalled lithotomy packs due to calibration issues with sterilization equipment that may compromise sterility assurance. Affected units were distributed nationwide and worldwide.
Product
Medline Convenience Kits: 1) LITHOTOMY PACK, Model Number: DYNJ83185; 2) LITHOTOMY PACK, Model Number: DYNJ83185A;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1408-2026·2026-02-25
Medline PPE Convenience Kit Sterilization Calibration Issue Recall
Medline is recalling approximately 7,575 PPE Convenience Kits (Model DYK1011945P) due to sterilization equipment calibration issues that may compromise device sterility. Affected products were distributed nationwide.
Product
Medline Convenience Kits: 1) PPE KIT, Model Number: DYK1011945P
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1411-2026·2026-02-25
Medline Convenience Kits Recalled Over Sterilization Equipment Calibration Issues
Medline is recalling 9,720 sterilized medical device kits due to sterilization equipment calibration problems that may compromise their sterility assurance levels.
Product
Medline Convenience Kits: 1) LVAD DRIVELINE TRAY, Model Number: DM1035A; 2) LVAD DRIVELINE TRAY, Model Number: DM1035; 3) CENTRAL LINE DRESSING CHANGE TRAY, Model Number: DT8670A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1396-2026·2026-02-25
Medline Endoscopy Kits Recalled Due to Sterilization Equipment Calibration Issues
Medline is recalling over 23,000 endoscopy procedure kits due to calibration issues with sterilization equipment that may affect the sterility assurance level of the devices.
Product
Medline Convenience Kits: 1) BAPTIST FLOYD ENDO GI KIT, Model Number: DYKE1455B; 2) GI LAB OTHER ENDO KIT, Model Number: DYKE1721
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1392-2026·2026-02-25
Medline Surgical and Biopsy Kits Recalled Due to Sterilization Equipment Calibration Issues
Medline is recalling 2,740 surgical and biopsy convenience kits due to calibration issues with sterilization equipment that may have compromised product sterility. No injuries have been reported.
Product
Medline Convenience Kits: 1) KIT SURG ONC EXCISION BREAST, Model Number: DYKMBNDL84A; 2) KIT SURG ONC EXPLORATORY LAP, Model Number: DYKMBNDL87A; 3) CT BIOPSY TRAY, Model Number: DYNDH1143C; 4) BIOPSY SPECIALS PACK, Model Number: DYNDH1873; 5) BIOPSY SPECIALS PACK, Model
Category
Medical Device
Distribution
Distributed nationwide