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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.
May 7, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits, labeled as: PLASTICS SUTURE TRAY, REF SUT13535
Hazard: It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.
May 7, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits, labeled as: 1) STERILE PREP KIT, REF DYNDA1359A; 2) STRL EK SINGLE PACK, REF DYNDA1360B;
Hazard: It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.
May 7, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits, labeled as: NON STERILE I&D KIT, REF DYKM1438
Hazard: It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.
May 7, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits, labeled as: T AND A PACK -LF, REF DYNJ85792
Hazard: It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.
May 7, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Sterile 0.9% Normal Saline, USP, 100mL, REF RDI30296
Hazard: It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.
May 7, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Sterile Water, USP, 100mL, REF RDI30295
Hazard: It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) ARTHROSCOPIE DU GENOU-LF, Model Number: DYNJ40229A; 2) ARTHR
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Refer to RES
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) BASIC CATARACT, Model Number: DYNJ41097A; 2) PK EYE, Model N
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) UTHET TYLER OB PACK, Model Number: DYNJ68673; 2) D AND C PAC
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) PERI GYN PACK, Model Number: DYNJ80786; 2) D & C HYSTEROSCOP
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) ED CRASH C-SECTION TRAY, Model Number: MNS13635A; 2) C-SECTI
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) STANDARD D&C, Model Number: DYNJ69733; 2) NHS - LAP BOWEL GN
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) CW PERI GYN, Model Number: DYNJ80807B
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) LABOR AND DELIVERY PACK-LF, Model Number: DYNJ26971L; 2) VAG
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) NEURO PACK WRO-LF, Model Number: DYNJ41856C; 2) STIM IMPLANT
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) HERNIA REPAIR TOTE, Model Number: DYNJ908337C
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) UNIVERSAL DRAPE PACK, Model Number: DYNJCD0239
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) CSTM PACEMAKER DRAPE PACK, Model Number: DYNJCD0339
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) SKIN LESION SET, Model Number: MNS6270
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) NAIL PACK, Model Number: SUT15830A;
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) IV PACK SOUTH, Model Number: DYNJ88422
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) PRECIP TRAY, Model Number: MNS12590
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Refer to RES
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) MINOR BASIN -SMH, Model Number: DYNJ907733B
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) OCULOPLASTIC PICK PACK, Model Number: DYNJ43914B; 2) PLASTIC
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) T&A ENDO PACK, Model Number: DYNJ59620A; 2) TRAY ADD A CATH
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Refer to RES
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) T A PACK, Model Number: DYNJ67791A; 2) NASAL PACK, Model N
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) RHINOPLASTY PACK, Model Number: DYNJ27333F
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.