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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 9, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. OPEN H
Hazard: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
August 9, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. ELECTR
Hazard: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
August 9, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. AAA PA
Hazard: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
August 9, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. MULTI-
Hazard: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
August 9, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. CRMC M
Hazard: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
August 9, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. (13) S
Hazard: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
August 9, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. ANGI
Hazard: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
August 9, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. ANGI
Hazard: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
August 9, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as PEDIATRIC EP PACK, Model N
Hazard: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
August 9, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a.18G CP
Hazard: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
August 9, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. ART L
Hazard: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
August 9, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. ANEST
Hazard: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
August 9, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Probe Cover Kits containing Turkuaz Ultrasound Gel, Labeled as the following: a. COVER, PROBE, W/GEL AND BAN
Hazard: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
August 2, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs
Hazard: The case and each (i.e. packet) labels for the DYND3000xxP series do not include an expiration date, however, the lubricating jelly (MDS032280) included in the DYNDP3000xxP series is labeled with an expiration date.
July 26, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline O.R. Scissors, S/B, Sterile, 5.5, Model #DYND04000
Hazard: The scissors were manufactured without a tip protector resulting in the scissors breaking through the semi-rigid plastic tray compromising sterility.
July 26, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) TOTAL JOINT, Model Number CDS9
Hazard: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
July 26, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: KIT,SUCTION CATH,14FR W/WATER, Mo
Hazard: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
July 26, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: BREAST BIOPSY TRAY, Model Number
Hazard: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
July 26, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) CVC INFANT INSERTION PACK, Mod
Hazard: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
July 26, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: PROBE COVER PACK, Model Number
Hazard: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
July 26, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) ARTERIAL LINE START KIT , Mode
Hazard: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
July 26, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) FEMORAL ARTERIAL LINE BUNDLE,
Hazard: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
July 26, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) ULTRASOUND PACK, Model Number
Hazard: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
July 26, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: DIALYSIS ACCESSORY PACK W/O CATHE
Hazard: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
July 26, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) VNUS TRAY, Model Number DYNJ44
Hazard: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
July 26, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) CATHETERLESS INSERTION KIT, M
Hazard: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
July 26, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) VANTEX CVC BNDL, 3L 7F 16CM W M
Hazard: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
July 26, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) RADIAL ARTERIAL LINE KIT, Mode
Hazard: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
July 26, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: ARTHROSCOPY PACK, Model Number
Hazard: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
July 26, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) CRANIOTOMY CDS-1, Model Numb
Hazard: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.