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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
21
22
23
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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.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing semi-rigid suction liners labeled as follows: a) AMB VITRECTOMY, Pack Number DYNJ
Hazard: XXX
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing semi-rigid suction liners labeled as follows: MERCY TIFFIN C-SECTION, Pack Number D
Hazard: Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing semi-rigid suction liners labeled as follows: MTHZ GYN LAPAROSCOPY, Pack Number DYN
Hazard: Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing semi-rigid suction liners labeled as follows: KIT NEURO SHUNT ST LOUIS CHILD, Pack N
Hazard: Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing semi-rigid suction liners labeled as follows: ANES TURNOVER KIT-LF, Pack Number DYN
Hazard: Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing semi-rigid suction liners labeled as follows: NICU ADMIT KIT, Pack Number DYKA1014G
Hazard: Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing semi-rigid suction liners labeled as follows: a) ENDO KIT, Pack Number DYKE1092B;
Hazard: Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing semi-rigid suction liners labeled as follows: a) MINOR BREAST, Pack Number DYNJ90
Hazard: Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing semi-rigid suction liners labeled as follows: a) ENDO KIT, Pack Number DYKE1350D;
Hazard: Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing semi-rigid suction liners labeled as follows: a) ENDO BRONCH PACK, Pack Number DYKE
Hazard: Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing semi-rigid suction liners labeled as follows: a) MINOR PROCEDURE, Pack Number CDS98
Hazard: Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing semi-rigid suction liners labeled as follows: a) BAPTIST FLOYD BRONCHOSCOPY, Pack N
Hazard: Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing semi-rigid suction liners labeled as follows: DENTAL, Pack Number DYNJ909451A
Hazard: Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing semi-rigid suction liners labeled as follows: a) OPEN HEART KIT,ALTA BATES HOSP,
Hazard: Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing semi-rigid suction liners labeled as follows: a) ANESTHESIA CIRCUIT-LF, Pack Number
Hazard: Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Semi-rigid suction liners labeled as follows: a) SEMI RIGID SUCTION LINER, REF OR515; b) SEMI RIGID SUCTION L
Hazard: Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline ReNewal Reprocessed Ethicon Harmonic ACE+7 Shears w/ Adv. Hemostasis Use Only w/GEN11 SW v2018-1 and Lower 5mm x
Hazard: Potential for an incomplete seal on the packaging tray.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline ReNewal Reprocessed Covidien LigaSure Impact, Sealer/Divider, Nano-Coated, Compatible w/ FT10 18cm FT10 SW Versi
Hazard: Potential for an incomplete seal on the packaging tray.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider, Nano-Coated, Compatible w/ FT10 37 cm FT10 SW
Hazard: Potential for an incomplete seal on the packaging tray.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline ReNewal Reprocessed Covidien LigaSure Blunt Tip, Sealer/Divider, Nano-Coated, Compatible w/ FT10 37cm FT10 SW Ve
Hazard: Potential for an incomplete seal on the packaging tray.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls ANESTHESIA TURNOVER KIT, Pack Number DYNJAA0377A
Hazard: A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that the user assumes sterility during its use, there is an increased risk of patient infection.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls ANESTHESIA TURNOVER KIT, Pack Number DYNJAA0377
Hazard: A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that the user assumes sterility during its use, there is an increased risk of patient infection.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls KIT PEDI CRANI LAMI, Pack Number DYNJ907372A
Hazard: A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that the user assumes sterility during its use, there is an increased risk of patient infection.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls CRANIOTOMY PACK, Pack Number DYNJ46552O
Hazard: A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that the user assumes sterility during its use, there is an increased risk of patient infection.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits, labeled as: aa1) BURN PACK-LF, Pack Number DYNJ0781678S ; 2) BURN PACK , Pack Number DYN
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.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits, labeled as: 1) KNEE ARTHROSCOPY CDS-LF , Pack Number CDS983874F ; 2) HAND, Pack Number C
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.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits, labeled as: 1) BLOOD CULTURE COLLECTION KIT, Pack Number BP115; 2) NICU CNTRL LINE BLOOD
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.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits, labeled as: BIOPSY TRAY-LF, Pack Number DYNDH1229
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.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits, labeled as: GAMMA NAIL CDS-LF , Pack Number CDS983505K
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.
September 18, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits, labeled as: 1) SUTURING SET PACK ASSY P791011, Pack Number 59112; 2) SUTURE SET, Pack Nu
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.