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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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25
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. FETA
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. KIT
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. PROB
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. DR 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. DBD-
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. PREM
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. CVC
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. CENT
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. ADUL
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. 18GX6"
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. PEDIAT
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. DR. RO
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. 7F, 20
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. CATH
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. (54)
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. CVC
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. CENT
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. PACK
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. DIAL
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. ABLA
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. LIVE
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. DBD-
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. CARO
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 STERILE SET FOR IMPLANT-LF
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. ABLA
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. SHY
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. A V FI
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. 16CM
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. VASC
Hazard: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.