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.

226–250 of 351

ModerateFDA (Devices)·Z-1389-2026·2026-02-25
Medline surgical and catheterization kits recalled for sterilization calibration issues
Medline is recalling 30,958 Convenience Kits for surgical and catheterization procedures due to calibration issues with sterilization equipment that could compromise sterility assurance levels.
Product
Medline Convenience Kits: 1) OR ARTERIOGRAM, Model Number: CDS985094F; 2) KIT SURG ONC LAP DIAG/CV CATH, Model Number: DYKMBNDL153; 3) KIT ACES INSERT PERCUTANEOUS T, Model Number: DYKMBNDL4A; 4) KIT ACES INSERT PERCUTANEOUS T, Model Number: DYKMBNDL4B; 5) VEIN PROCEDURE
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1324-2026·2026-02-18
Reprocessed Diagnostic Ultrasound Catheters Recalled for Residual Particles
Reprocessed Biosense Webster SOUNDSTAR eco diagnostic ultrasound catheters may contain residual particles that could cause blood clots or infection. Medline Industries is recalling 94 units distributed nationwide.
Product
Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheters: Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on GE Systems 10439072RH; Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on Siemens Systems 10438577RH; Bios
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1321-2026·2026-02-18
Reprocessed Livewire Electrophysiology Catheters Recalled for Contamination Risk
Medline Industries is recalling reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters nationwide due to potential contamination with residual material particles that may cause serious infections or blood clots.
Product
Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters: Livewire Steerable Electrophysiology Catheter,10 Elec. 2-5-2mm 401582RH 401940RH; Livewire Steerable Electrophysiology Catheter,20 Elec. 2-10-2mm 401904RH; Livewire Steerable Electrophysiology Cath
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1323-2026·2026-02-18
Medline Reprocessed ICE Catheters Recalled for Residual Material
Medline Industries is recalling 650 units of ReNewal Reprocessed ViewFlex Xtra ICE Catheters due to contamination with residual material particles. These defective devices pose a risk of serious infection and life-threatening blood clots.
Product
Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter 9F x 90cm D087031RH 20197344019554¿
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1320-2026·2026-02-18
Reprocessed diagnostic catheters recalled for residual material contamination
Medline Industries recalls reprocessed Abbott diagnostic catheters that may contain particles of residual material. Use could cause infection, inflammatory response, blood clots, or embolism.
Product
Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm 81105RH 81172RH; Abbott Inquiry Steerable Diagnostic Catheter 20 Elec. 2-10-2mm 81202RH; Abbott Inquiry Steerable Diagnostic Catheter 4 Elec. 5mm
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1325-2026·2026-02-18
Reprocessed Siemens ACUSON AcuNav Ultrasound Catheters Recalled for Particle Contamination
Medline Industries is recalling 511 reprocessed Siemens ACUSON AcuNav ultrasound catheters due to residual material particles. These particles may cause systemic infection, blood clots, or embolism.
Product
Reprocessed Siemens ACUSON AcuNav Diagnostic Ultrasound Catheters: ACUSON AcuNav Ultrasound Catheter, Use on GE Systems 10135910RH; 10043342RH ACUSON AcuNav Ultrasound Catheter, Use on Siemens Systems 10135936RH, 08255790RH
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1319-2026·2026-02-18
Medline Reprocessed Cardiac Catheters Recalled for Particle Contamination Risk
Medline reprocessed cardiac catheters may contain residual material particles, risking systemic infection, blood clots, and embolism. Affected units should be immediately quarantined and returned.
Product
Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10 Electrodes 2-8-2mm Spacing w/AutoID w/ EZ Steer BD710DF282CRH; Webster CS Catheter 10 Electrodes, 2-8-2mm Spacing w/ EZ Steer BD710DF282RRH BD710FJ282RRH; Webster CS Catheter 10 Electrodes, 2-8-2mm S
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1322-2026·2026-02-18
Reprocessed electrophysiology catheters recalled for residual material contamination
Medline Industries is recalling 48 units of reprocessed St. Jude diagnostic electrophysiology catheters due to residual material that may cause systemic infection, blood clots, or embolism.
Product
Reprocessed St. Jude Supreme and Response Diagnostic Electrophysiology Catheters: St. Jude Medical Supreme Diagnostic Electrophysiology Catheter 4 Elec. 2-5-2mm 401211RH 401222RH 401223RH 401226RH 401227RH 401260RH 401261RH 401306RH 401309RH 401312RH 401430RH 40143
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1326-2026·2026-02-18
Medline Anesthesia Artline Packs Recalled for Potential Packaging Defects
Medline Industries is recalling 120 Anesthesia Artline medical convenience kits due to BD ChloraPrep Triple Swabsticks with potentially open seals. Open packaging could compromise product sterility.
Product
Medline medical convenience kits packaged as: ANESTHESIA ARTLINE PACK, Kit SKU DYNJ47387B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1328-2026·2026-02-18
Medline pediatric catheter securement kits recalled for potential open packaging seals
Medline Industries is recalling 450 pediatric catheter securement dressing kits nationwide due to potential open seals on BD ChloraPrep applicator packaging. Open seals may compromise product sterility and integrity.
Product
Medline medical convenience kits packaged as: PEDIATRIC CATH SECUREMENT DRSG, Kit SKU DYNDC3108
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1312-2026·2026-02-18
Medline Suction Catheter Kits Recalled for Wrong Size Catheter
Medline 14 Fr Suction Catheter Kits may contain an 8 Fr catheter instead, potentially causing airway obstruction and respiratory failure. The kits were distributed nationwide and in Canada.
Product
Medline 14 Fr Suction Catheter Kits SKU DYND40972 - respiratory convenience kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1331-2026·2026-02-18
Medline Medical Convenience Kits Recalled for Unsealed Applicators
Medline Industries recalls 7,380 medical convenience kits nationwide due to potentially open seals on BD ChloraPrep Triple Swabstick applicators, which could affect product sterility.
Product
Medline medical convenience kits packaged as: 1) POWERGLIDE DRESSING CHANGE KIT, Kit SKU DYNDH1576; 2) CENTRAL LINE TRAY W/ CHLRP SWB, Kit SKU RWM-DC57KC.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1327-2026·2026-02-18
Medline Catheter Securement Kits Recalled for Potentially Open Applicator Seals
Medline Industries is recalling 1,350 Adult Cath Securement Dressing Kits with potentially open seals on BD ChloraPrep Triple Swabstick applicators. Open packaging may compromise product sterility.
Product
Medline medical convenience kits packaged as: ADULT CATH SECUREMENT DRSG, Kit SKU DYNDC3109
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1333-2026·2026-02-18
Medline Blood Culture Kit Recall Due to Open Applicator Seal
Medline Industries is recalling 4,300 Blood Culture Kits due to open seals on applicator packaging that could compromise sterility and introduce contamination during specimen collection.
Product
Medline medical convenience kits packaged as: BLOOD CULTURE KIT NS, Kit SKU DYNDH2088
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1336-2026·2026-02-18
Medline Circumcision Kit Applicators Recalled for Open Packaging Seals
Medline is recalling specific circumcision kits due to potentially open seals on sterile applicators that could compromise sterility. This affects 168 units distributed nationwide.
Product
Medline medical convenience kits packaged as: MERCY CIRCUMCISION TRAY, Kit SKU CIT6135B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1330-2026·2026-02-18
Medline Medical Kits Recalled Due to Potentially Open Applicator Packaging
Medline Industries is recalling 21,854 units of sterile medical device kits containing ChloraPrep Triple Swabsticks due to potential open seals on applicator packaging. No illnesses have been reported.
Product
1) UNIVERSAL KIT, Kit SKU DT22010B; 2) VAD ACCESS KIT, Kit SKU DT22790C; 3) VAD ACCESS KIT, Kit SKU DT22790C; 4) PROCEDURE TRAY, Kit SKU DYNDA2966A; 5) PROCEDURE TRAY, Kit SKU DYNDA2966A; 6) PEDIATRIC CENTRAL LINE SMALL, Kit SKU DYNDC2208C; 7) PORT DRESSING KIT, Kit S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1335-2026·2026-02-18
Medline Medical Kits Recalled Due to Potential Open Packaging Seals
Medline Industries is recalling 216 medical convenience kits containing BD ChloraPrep Triple Swabsticks due to potential open seals on applicator packaging that may compromise product sterility.
Product
Medline medical convenience kits packaged as: STERILE RESUTURE PACK, Kit SKU DYNDL1980A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1313-2026·2026-02-18
Intubation Tray recalled for incorrect suction catheter size risk
Medline Industries is recalling Intubation Trays (SKU DYNJAA245B) distributed nationwide and in Canada because smaller 8 Fr suction catheters were packed instead of required 14 Fr catheters, which may cause airway obstruction and respiratory failure.
Product
Intubation Tray (Adult) containing Suction Catheter Kits SKU DYNJAA245B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1334-2026·2026-02-18
Medline Medical Kits With BD ChloraPrep Swabsticks Recalled for Open Packaging Seals
Medline Industries is recalling 8,445 medical convenience kits nationwide due to open seals on BD ChloraPrep Triple Swabstick applicator packaging. The defect may compromise product sterility.
Product
Medline medical convenience kits packaged as: ) LVAD DRESSING CHANGE TRAY, Kit SKU DM320C; 2) PORT AND IO ACCESS DRESSING KI, Kit SKU DT15780A; 3) PORT-A-CATH DRESSING CHANGE TR, Kit SKU DT16615; 4) LARGE BORE CENTRAL LINE DRSG C, Kit SKU DT19660; 5) CENTRAL LINE DRESS
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1332-2026·2026-02-18
Medline Suture Removal Trays Recalled Due to Potentially Open Packaging Seals
Medline Industries is recalling 2,448 suture removal kits due to potentially open packaging seals on BD ChloraPrep Triple Swabsticks applicators, which could compromise sterility.
Product
Medline medical convenience kits packaged as: SUTURE REMOVAL TRAY, Kit SKU DYNDR1277A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1329-2026·2026-02-18
Medline medical convenience kits recalled for open seals on applicators
Medline Industries is recalling 7,570 medical convenience kits containing BD ChloraPrep Triple Swabsticks due to potentially open seals on applicator packaging. The kits are distributed nationwide to hospital and clinical settings.
Product
Medline medical convenience kits packaged as: 1) CANCER SERVICE PORT KIT, Kit SKU DT22710; 2) LINE KIT, Kit SKU DYNDA1857A; 3) PICC REMOVAL KIT, Kit SKU DYNDC1978A; 4) PORT ACCESS TRAY, Kit SKU DYNDC2367; 5) NICU CENTRAL LINE TRAY, Kit SKU DYNDC2407B; 6) CVC DRESSING
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1197-2026·2026-02-04
Medline surgical procedure kits recalled for defective adhesive vial tubing
Medline is recalling 1,928 medical procedure convenience kits due to defective tubing in MASTISOL liquid adhesive vials that may crack during use. The kits were distributed nationwide to healthcare facilities.
Product
Medline medical procedure convenience kits labeled as: 1) RR-GYN LAPAROSCOPY PACK-LF, Kit SKU DYNJ0395022O; 2) PELVISCOPY PACK-LF, Kit SKU DYNJ0415776Q; 3) DIVA PACK, Kit SKU DYNJ04811O; 4) DA VINCI PROSTATE/COLPOPEXY, Kit SKU DYNJ44864S; 5) MH ROBOTICS PACK, Kit SKU D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1193-2026·2026-02-04
Medline Medical Procedure Convenience Kits Recalled for Cracking Tubing Defect
Medline medical procedure convenience kits containing MASTISOL liquid adhesive are recalled due to reports that the butyrate tubing in the adhesive vials cracks during use. Approximately 857 units were distributed nationwide.
Product
Medline medical procedure convenience kits labeled as: 1) DRAWER 1 AIRWAY, Kit SKU ACC010270A; 2) DRAWER 2, Kit SKU ACC010690; 3) DRAWER 3 SYR/DRS/MON/NG 1 OF 3, Kit SKU ACC011073; 4) HYPOSPADIUS PACK, Kit SKU DYNJ00282Q; 5) SJ NEURO PACK RFID-LF, Kit SKU DYNJ0101360K;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1194-2026·2026-02-04
Medline HEAD SHAVE-LATEX SAFE KIT recalled for cracking tubing defect
Medline HEAD SHAVE-LATEX SAFE KIT kits are being recalled due to complaints that the MASTISOL liquid adhesive tubing cracks during use, potentially causing adhesive leakage.
Product
Medline medical procedure convenience kits labeled as: HEAD SHAVE-LATEX SAFE KIT, Kit SKU P903933B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1188-2026·2026-02-04
Medline Cardiac Procedure Kits Recalled Due to Cracking Tubing in Adhesive Vials
Medline Industries recalls eight medical procedure kits nationwide due to MASTISOL liquid adhesive vials with cracking butyrate tubing. The defect could affect proper device function during cardiac and vascular procedures.
Product
Medline medical procedure convenience kits labeled as: 1) PACER / CATH LAB PACK-LF, Kit SKU DYNJ0972604A; 2) PACEMAKER/ICD PACK, Kit SKU DYNJ33822L; 3) VENOUS ACCESS PACK, Kit SKU DYNJ45640B; 4) PACEMAKER SET UP, Kit SKU DYNJ63377D; 5) PACK PACEMAKER CUSTOM,9909178, Ki
Category
Medical Device
Distribution
Distributed nationwide