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MEDLINE INDUSTRIES, LP - Northfield Recalls
822 recalls on record · December 29, 2021 to October 1, 2025 · 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.
August 28, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls LINER, SOFT, SUCTION CANISTER, 1500CC, REF DYNDSCL1500
Hazard: A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
August 14, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion procedure kits labeled as: 1) CVC INSERT BUNDLE 16CM, Pack Number ECVC3260; 2) CVC DOUBLE LUMEN 16CM, Pac
Hazard: Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
August 14, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion procedure kits labeled as NEURO ANGIO PACK, Pack Number DYNDA1431A
Hazard: Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
August 14, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits labeled as: 1) WMC HYBRID OR PACK PART 1 , Pack Number CMPJ08068F ; 2) VASCULAR PACK , Pack
Hazard: Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
August 14, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits labeled as: 1) NEPHROLOGY PACK, Pack Number DYNJ59089; 2) NERVE BLOCK TRAY, P
Hazard: Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
August 14, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits labeled as: 1) CONTINUOUS BLOCK, Pack Number DYNJRA0960C; 2) COMBINED SPINAL AND EPIDURAL, P
Hazard: Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
July 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Non-sterile convenience kits: a. Medline CC Drawer 4 IV Circulation, Pack #ACC010254B, containing a Pure Pouch compon
Hazard: Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
July 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Non-sterile convenience kits: Medline Open Heart CDS, Pack #CDS981759C, containing a Pure Pouch with component Reorde
Hazard: Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
July 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Non-sterile convenience kits: a. Medline Difficult Airway Tray W/O Cook, Pack #ACC010578, containing a Pure Pouch wi
Hazard: Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
July 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Nonsterile convenience kits: a. Medline Delivery, Pack #DYNJ901130I, containing a Pure Pouch with component Reorder
Hazard: Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
July 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile convenience kits: a. Medline Retrograde PK-22025203-LF, Pack #DYNJ47873K, containing a Pure Pouch containing
Hazard: Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
July 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile convenience kit: Medline Birthing Room Pack, Pack #DYNJ38429D, containing a Pure Pouch component Sterile Shar
Hazard: Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
July 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile surgical convenience kit: Medline Neuro IR Pack, Pack #DYNJ56073C, containing a Pure Pouch with component Me
Hazard: Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
July 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile surgical convenience kit: Medline Retrograde PK-22025203-LF, Pack #DYNJ47873L, containing a Pure Pouch with c
Hazard: Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
July 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile surgical convenience kits: a. Medline Cath Lab Special Procedure, Pack #00-RDF0360, containing a Pure Pouch
Hazard: Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
June 12, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE STERILE IRIS SCISSORS CVD/STD REF DYNJ04049 (case) and DYNJ04049H (individual unit)
Hazard: There is the potential of the tip protector to fall off 4.5" sterile, curved, Iris Scissors
June 12, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE LUER SLIP DISPOSABLE SYRINGE WITHOUT NEEDLE, REF SYR101020
Hazard: It has been identified that testing documentation does not support that the syringes can successfully deliver accurate volumes across the full range of their claimed graduated capacity and may pose a risk to patient health.
June 12, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE LUER LOCK DISPOSABLE SYRINGE WITHOUT NEEDLE, REF SYR101010
Hazard: It has been identified that testing documentation does not support that the syringes can successfully deliver accurate volumes across the full range of their claimed graduated capacity and may pose a risk to patient health.
June 12, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Syringes labeled as: a) SYR 10ML L/L CONTROL, Item Numbers: 1. DNSC91881, 2. DYNJSYRPPC10; b) SYRINGE 20ML BLUE
Hazard: These syringes were identified to be affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and other quality issues have been identified that may pose a risk to patient health.
June 5, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline medical procedure kits, labeled as follows: a) PARACERVICAL PUD TRAY, REF DYNDH1832; b) AHS PARACERVICAL/PU
Hazard: Trumpet Needle Guide ring can detach when excessive pressure is applied.
June 5, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion OB INSTRUMENT TRAY, REF MN3925; Medical procedure convenience tray
Hazard: Trumpet Needle Guide ring can detach when excessive pressure is applied.
June 5, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Sub-G Endotracheal Tube with Subglottic Suctioning: (1) REF DYNJ18860, Polyurethane Cuff 6.0 mm ID; (2) REF
Hazard: Complaints have been received that the device inflation tube detached and/or tore from the main tube, resulting in potential moisture buildup, loss of pressure, or inability to inflate. There were also reports the suction pump is difficult to connect or detaches during use.
May 22, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Namic FLUID DELIVERY SET, REF 91300040
Hazard: Products have a lack of sterility assurance.
May 22, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls namic CONVENIENCE KIT, a) CAROTID MANIFOLD KIT, REF 60011045; b) 3V MANIFOLD KIT ON WITH NAMIC DT & WASTE MANAGEMENT
Hazard: Products have a lack of sterility assurance.
April 17, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Bed Assist Bars, labeled as follows: a) Medline SwivAssist Bar, Model Number MDS6800SWIV (case of 3), b) Medline Sw
Hazard: Medline is recalling certain lots of our Adult Portable Bed Rails that were manufactured after the mandatory compliance requirement (ASTM F3186-17, Standard Specification for Adult Portable Bed Rails and Related Products and 16 CFR Part 1270, Safety Standard for Adult Portable Bed Rails) and failed to meet all mandatory requirements outlined in these standards.
April 17, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Bed Assist Bars, labeled as follows: a) Medline, Model Number BA6800, b) Medline Martha Stewart, Model Number MDS68
Hazard: Medline is recalling certain lots of our Adult Portable Bed Rails that were manufactured after the mandatory compliance requirement (ASTM F3186-17, Standard Specification for Adult Portable Bed Rails and Related Products and 16 CFR Part 1270, Safety Standard for Adult Portable Bed Rails) and failed to meet all mandatory requirements outlined in these standards.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Blood Pressure Unit, Model (REF) Numbers: a) MDS4001, b) MDS4001LA, c) MDS4001PLUS
Hazard: The firm provided a set of specifications for the device, but some units of the device were manufactured non-compliant with the specifications. However, the firms Receiving Dept. accepted these units into inventory
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE SWABSTICKS ALCOHOL 3PK, Product code DYNDA2723
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE 4.5 IN WIRE CUT SCISSORS, Product Code DYND04006
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE SWABSTICKS PVP 3 PK, Product Code DYNDA2724
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.