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Medline Industries Recalls
665 recalls on record · December 26, 2012 to August 19, 2026 · Drugs, Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes EYE PACK DYNJ35056A HEART
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes GU DAVINCI PACK - LF DYNJ90939
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ANGIO KIT PACK DYNJ50783B
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes Medline Convenience Kits conta
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes FACE/RHINOPLASTY PACK DYNJ8034
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BARIATRIC DYNJ905153M, DYNJ9
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes MINOR ENT SINUS PACK-LF
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BIOPSY PACK DYNJ38587A, DYNJ38
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes TAVR PACK DYNJ69246B ABDOMI
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ADULT CATH PACK-LF DYNJ38395G
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes JUDKINS PACK DYNJ51126 AN
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) ARTHROSCOPY PACK, Model Number: DYNJ82440
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) BWNBORO CRANIOTOMY PACK-LF, Model Number: DYNJ32841F; 2) CRANIOTOMY PACK-LF, Model Number: DYNJ46069
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) D AND C PACK, Model Number: DYNJ41254B
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) HYSTEROSCOPY PACK, Model Number: DYNJ48399C; 2) SLING PACK, Model Number: DYNJ62849B
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) GYN LAPAROSCOPY PACK, Model Number: DYNJ41257F
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) LABOR PACK-22025208-LF, Model Number: DYNJ44813D
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) ARTHROGRAM TRAY, Model Number: DYNJ07425; 2) TOL NEURO ANGIO PACK, Model Number: DYNJ38610I 3) ANGI
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) SYR CONTROL 8ML ROTATING, Model Number: DNSC89369; 2) SYRINGE 10ML CONTROL MLL, Model Number: DYNJSY
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) NEWBORN ADMISSION, Model Number: DYKB1038; 2) DRAINAGE TRAY, Model Number: DYNDA3188; 3) VA ORLAND
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) BREAST PACK, Model Number: DYNJ66777D
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) GENERAL LAPAROSCOPY, Model Number: CDS930027Y
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) ENT PACK, Model Number: DYNJ59030B; 2) ENT, Model Number: DYNJ908586C; 3) LH 3 PORT W/O WASTEBAG,
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) HEART TRANSPLANT BIOPSY, Model Number: DYNJ37543A
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) PICC TRAY, Model Number: DYNJ41648A
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) MTS LEFT HEART KIT-CAROLINAS HOS, Model Number: 60021775; 2) DBD-MTS LHK BHS BAPTIST. LOUISVI, Model
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) CATH LAB CDS, Model Number: CDS840228F; 2) IR PACK, Model Number: DYNDH2104; 3) CARDIAC CATH PACK-LF,
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) ANGIOGRAPHY PACK-LF, Model Number: DYNJQ0505M; 2) ANGIO PACK, Model Number: DYNJT2021G; 3) ANGIOGR
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) SYR CNTRL 10ML RING W/ROT NB, Model Number: DYNJSYR10CWRB; 2) MANIFOLD KIT LOW PRESSURE OFF, Model N
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) ANGIO CATH PACK-MARY IMMACULAT, Model Number: DYNJ24517D
Hazard: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.