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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.
December 20, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Leg bag, REF DYND12578
Hazard: Undeclared latex
December 20, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Leg bag, REF DYND12574
Hazard: Undeclared latex
December 20, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls STERILE POVIDONE, REF DYNDA2061
Hazard: The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.
December 20, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls STERILE BETADINE, REF DYNDA1998
Hazard: The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.
December 20, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls PVP SOLUTION SING STRL, REF DYNDA1858
Hazard: The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.
December 20, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls STERILE PVP, REF DYNDA1649
Hazard: The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.
December 20, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls STERILE STERILE PREP STICK, REF DYNDA1134
Hazard: The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.
December 20, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls STERILE PVP SLN KIT, REF DYNDM1097
Hazard: The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.
December 20, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls STERILE PVP SOLUTION, REF DYNDA1907
Hazard: The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.
November 22, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls BLOOD CULTURE KIT, REF DYNDH1647B
Hazard: This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.
November 22, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls 24 BLOOD CULTURE KIT, REF DYNDH1632
Hazard: This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.
November 22, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls CENTRAL LINE BLOOD CULTURE DRA, REF DYNDH1562
Hazard: This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.
November 22, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls PERIPHERAL BLOOD CULTURE DRAW, REF DYNDH1561
Hazard: This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.
November 22, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls ADLT BLOOD CULTURE COLLECT KIT, REF DYNDH1245
Hazard: This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.
November 15, 2023DrugsFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Clinical TREAT Antifungal Powder, Vanilla Scent, 3 OZ (85 g) tube, Active Ingredient: Miconazole Nitrate 2.0% w/w Antifu
Hazard: CGMP deviations: the product was shipped from the Manufacturer to a Medline warehouse and released to stock while it was still under investigation for low assay results on the active ingredient miconazole nitrate.
October 25, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE ReNewal Harmonic ACE+7 Shears w/ Adv. Hemostasis Use Only w/ GEN11 SW v2018-1 and Lower, REF HARH45R. surgical
Hazard: Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray.
October 25, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE ReNewal Ligasure Sealer/Divider Nano-Coated Compatible with FT10 Generator, REF LF4418CR. electrosurgical inst
Hazard: Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray.
October 25, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE ReNewal Ligasure Maryland Jaw Sealer/Divider Nano-Coated Complatible with FT10 Generator, REF LF1944CR. elec
Hazard: Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray.
October 25, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE ReNewal Ligasure Blunt Tip Sealer/Divider Nano-Coated Compatible with FT10 Generator, REF LF1844CR. electrosur
Hazard: Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray.
October 11, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion Sterile CirClamp with 1.45cm Bell Reprocessed, Reorder CR3145K, 1 per package, 12 per case.
Hazard: The kits incorrectly contain CirClamp subassembly 345CRSAK which results in the kits containing an incorrect bell and base size.
September 27, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE STERILE IRIS SCISSORS CVD/STD, REF DYNJ04049
Hazard: 4.5" Iris Scissors, Sterile, Curved (DYNJ04049) are being recalled due to the potential of the tip protector to fall off. The sharp tip of the scissors could compromise the sterile barrier system by puncturing large and/or small holes that may not be visible to the user.
September 20, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls HUDSON RCI Addipak, UNIT DOSE VIALS, 5mL Sterile 0.9% NaCl Solution for Inhalation USP. REF RHUD59U
Hazard: Product dispositioned for scrap for sterility failure investigation that was inadvertently shipped to customers.
August 16, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Total Hip Kit, REF DYNJ903275S; surgical convenience kit
Hazard: The prep solution included in the Total Hip Kit expires prior to the expiration date of the Kit.
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. BREA
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. 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. EGG
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. CUST
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. C V
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. CHN
Hazard: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.