--- title: "MEDLINE INDUSTRIES, LP - Northfield Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search MEDLINE INDUSTRIES, LP - Northfield recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/medline-industries-lp-northfield/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # MEDLINE INDUSTRIES, LP - Northfield recall records **809** reported ongoing 822 records in this archive. Latest source date Jul 25, 2025. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Jul 25, 2025 FDA device enforcement ### [Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY, Kit Number ACC010369B; 2. ADULT ICU INTUBATION TRAY, Kit Number ACC010379A; 3. INTUBATION TRAY, Kit Number...](https://isitonrecall.com/recall/fda-device-z-2566-2025-medline-medical-convenience-kits-labeled-as-1-adult-intubation-tray-kit-number-acc010369b-2-adult-ic/) Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to the failure of the light to illuminate as intended. Class I Reported ongoing Distribution: US distribution to: AL, CA, DE, OR, TN, TX [Official source for Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY, Kit Number ACC010369B; 2. ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2566-2025%22) Jul 25, 2025 FDA device enforcement ### [Medline medical convenience kits labeled as: 1. NEWBORN RESUSCITATION KIT, Kit Number ACC010381C; 2. DRAWER 5 - POSITION 3, Kit Number ACC010532; 3. DRAWER #4C ADULT, Kit Number...](https://isitonrecall.com/recall/fda-device-z-2567-2025-medline-medical-convenience-kits-labeled-as-1-newborn-resuscitation-kit-kit-number-acc010381c-2-draw/) Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to the failure of the light to illuminate as intended. Class I Reported ongoing Distribution: US distribution to: AL, CA, DE, OR, TN, TX [Official source for Medline medical convenience kits labeled as: 1. NEWBORN RESUSCITATION KIT, Kit Number ACC010381C;...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2567-2025%22) Jul 23, 2025 FDA device enforcement ### [Medline Kits containing BD SureStep Foley Tray Systems: SKU/Description: CDS984076J GYN ROBOTIC DYNJG001004A LAVH MINOR DYNJG901001B CRANIOTOMY DYNJ908819B KIT CRANIOTOMY (only ...](https://isitonrecall.com/recall/fda-device-z-2479-2025-medline-kits-containing-bd-surestep-foley-tray-systems-sku-description-cds984076j-gyn-robotic-dynjg0/) Kits contain SureStep Foley Tray Systems recalled by BD that include incorrect product information insert sheets. If a mislabeled tray is used, patient risk ranges from minor injury to injury that requires medical intervention, such as infection or local/sy... Class II Reported ongoing Distribution: Domestic distribution to FL and IL. No OUS distribution reported. [Official source for Medline Kits containing BD SureStep Foley Tray Systems: SKU/Description: CDS984076J GYN ROBOTIC D...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2479-2025%22) Jul 14, 2025 FDA device enforcement ### [Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic Electrophysiology Catheter Models 401150RH, 401206RH, 401207RH, 401210RH, 401211RH, 401212RH, 401222...](https://isitonrecall.com/recall/fda-device-z-2460-2025-medline-renewal-reprocessed-st-jude-medical-response-and-supreme-diagnostic-electrophysiology-cathet/) Specific lots of reprocessed electrophysiology catheters may contain small residual particulates. Class I Reported ongoing Distribution: US Nationwide. [Official source for Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic Electrophysiology Ca...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2460-2025%22) Jul 8, 2025 FDA device enforcement ### [The Medline General Surgery Tray is customized to meet requirements of the hospitals and health care professionals utilizing them. The kit is provided sterile, single-use and in...](https://isitonrecall.com/recall/fda-device-z-2452-2025-the-medline-general-surgery-tray-is-customized-to-meet-requirements-of-the-hospitals-and-health-care/) Affected kits contain recalled Stryker Color Cuff Sterile Disposable Tourniquet Cuffs. Stryker Instruments initiated this recall due to a potential manufacturing defect in which the flange may detach from the bladder at the welded connection point. This det... Class II Reported ongoing Distribution: US Nationwide distribution tin the states of CA, FL, IA, and TX. [Official source for The Medline General Surgery Tray is customized to meet requirements of the hospitals and health c...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2452-2025%22) Jul 7, 2025 FDA drug enforcement ### [Medline Alcohol Prep Pads, 70% Isopropyl Alcohol, 100 Sterile 2-Ply Pads, Single Use Only, Large, www.medline.com, Manufactured for Medline Industries, LP, Three Lakes Drive, No...](https://isitonrecall.com/recall/fda-drug-d-0600-2025-medline-alcohol-prep-pads-70-isopropyl-alcohol-100-sterile-2-ply-pads-single-use-only-large-www-medl/) Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. Class II Reported ongoing Distribution: Nationwide [Official source for Medline Alcohol Prep Pads, 70% Isopropyl Alcohol, 100 Sterile 2-Ply Pads, Single Use Only, Large,...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0600-2025%22) Jul 7, 2025 FDA drug enforcement ### [CURAD Alcohol Prep Pads, Sterile, Medium, 2-Ply, Contents: 5 boxes per Carton, 30 Boxes per Case, Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, No...](https://isitonrecall.com/recall/fda-drug-d-0601-2025-curad-alcohol-prep-pads-sterile-medium-2-ply-contents-5-boxes-per-carton-30-boxes-per-case-single-us/) Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. Class II Reported ongoing Distribution: Nationwide [Official source for CURAD Alcohol Prep Pads, Sterile, Medium, 2-Ply, Contents: 5 boxes per Carton, 30 Boxes per Case,...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0601-2025%22) Jul 7, 2025 FDA drug enforcement ### [ReliOn, Sterile Alcohol Swabs, Skin Cleanser, 200 Swabs, Distributed by, Walmart, Inc., Bentonville, AR 72716 Walmart: 200 eaches per box, 24 boxes per case (4,800 eaches per ca...](https://isitonrecall.com/recall/fda-drug-d-0602-2025-relion-sterile-alcohol-swabs-skin-cleanser-200-swabs-distributed-by-walmart-inc-bentonville-ar-72716/) Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. Class II Reported ongoing Distribution: Nationwide [Official source for ReliOn, Sterile Alcohol Swabs, Skin Cleanser, 200 Swabs, Distributed by, Walmart, Inc., Bentonvil...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0602-2025%22) Jul 7, 2025 FDA drug enforcement ### [H-E-B, inControl, Sterile\* Alcohol Pads, CONT. 100 PADS, Packaged in China with components from Taiwan, Elaborado Con Orgullo Y Cuidado PARA H-E-B, San Antonio, TX 78204, NDC 37...](https://isitonrecall.com/recall/fda-drug-d-0603-2025-h-e-b-incontrol-sterile-alcohol-pads-cont-100-pads-packaged-in-china-with-components-from-taiwan-ela/) Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. Class II Reported ongoing Distribution: Nationwide [Official source for H-E-B, inControl, Sterile\* Alcohol Pads, CONT. 100 PADS, Packaged in China with components from T...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0603-2025%22) Jul 7, 2025 FDA drug enforcement ### [Good Neighbor Pharmacy, Alcohol Prep Pads, Distributed By AmeriSource Bergen, 1 West First Avenue, Conshohocken, PA 19428, Made in China: 100 eaches per box, 30 boxes per case, ...](https://isitonrecall.com/recall/fda-drug-d-0604-2025-good-neighbor-pharmacy-alcohol-prep-pads-distributed-by-amerisource-bergen-1-west-first-avenue-consh/) Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. Class II Reported ongoing Distribution: Nationwide [Official source for Good Neighbor Pharmacy, Alcohol Prep Pads, Distributed By AmeriSource Bergen, 1 West First Avenue...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0604-2025%22) Jul 7, 2025 FDA drug enforcement ### [RITE AID PHARMACY, first aid alcohol prep pads, DISTRIBUTED BY: RITE AID. 200 NEWBERRY COMMONS, ETTERS, PA 17319, NDC 11822-5156-2.](https://isitonrecall.com/recall/fda-drug-d-0605-2025-rite-aid-pharmacy-first-aid-alcohol-prep-pads-distributed-by-rite-aid-200-newberry-commons-etters-pa/) Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. Class II Reported ongoing Distribution: Nationwide [Official source for RITE AID PHARMACY, first aid alcohol prep pads, DISTRIBUTED BY: RITE AID. 200 NEWBERRY COMMONS, E...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0605-2025%22) Jun 16, 2025 FDA device enforcement ### [SwabFlush Prefilled Syringe with ICU Medical SwabCaps, 10mL Model no. EMZE010301](https://isitonrecall.com/recall/fda-device-z-2199-2025-swabflush-prefilled-syringe-with-icu-medical-swabcaps-10ml-model-no-emze010301/) SwabFlush syringes are affected by the ICU Medical recall of their SwabCap Disinfecting Cap due to a manufacturing issue which affects the seal between the foil lid and plastic container of the Swab Cap. The issue may result in a reduced level of disinfecti... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Canada and Panama. [Official source for SwabFlush Prefilled Syringe with ICU Medical SwabCaps, 10mL Model no. EMZE010301](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2199-2025%22) Jun 12, 2025 FDA device enforcement ### [Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: LABOR TRIAGE KIT, REF DYKM1564](https://isitonrecall.com/recall/fda-device-z-2153-2025-medline-convenience-kits-containing-bd-chloraprep-clear-1ml-applicator-labeled-as-labor-triage-kit-r/) Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms f... Class II Reported ongoing Distribution: Distributed domestically to California, Florida, Pennsylvania, and Texas. No international distribution. [Official source for Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: LABOR TRIA...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2153-2025%22) Jun 12, 2025 FDA device enforcement ### [Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: IV START KIT LAB DRAW-SH, REF CDS860014P](https://isitonrecall.com/recall/fda-device-z-2154-2025-medline-convenience-kits-containing-bd-chloraprep-clear-1ml-applicator-labeled-as-iv-start-kit-lab-d/) Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms f... Class II Reported ongoing Distribution: Distributed domestically to California, Florida, Pennsylvania, and Texas. No international distribution. [Official source for Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: IV START K...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2154-2025%22) Jun 12, 2025 FDA device enforcement ### [Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: 1) BLOOD CULTURE KIT, REF DYNDH1462B; 2) BLOOD CULTURE KIT, REF DYNDH1622C; 3) BLOOD CULTR...](https://isitonrecall.com/recall/fda-device-z-2155-2025-medline-convenience-kits-containing-bd-chloraprep-clear-1ml-applicator-labeled-as-1-blood-culture-ki/) Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms f... Class II Reported ongoing Distribution: Distributed domestically to California, Florida, Pennsylvania, and Texas. No international distribution. [Official source for Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: 1) BLOOD C...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2155-2025%22) Jun 12, 2025 FDA device enforcement ### [Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: C-SECTION PREP, REF DYNJ32702B](https://isitonrecall.com/recall/fda-device-z-2156-2025-medline-convenience-kits-containing-bd-chloraprep-clear-1ml-applicator-labeled-as-c-section-prep-ref/) Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms f... Class II Reported ongoing Distribution: Distributed domestically to California, Florida, Pennsylvania, and Texas. No international distribution. [Official source for Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: C-SECTION ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2156-2025%22) May 23, 2025 FDA device enforcement ### [Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: 1) CC DRAWER 4 IV CIRCULATION, REF ACC010254B; 2) CC ADULT DRAWER 2, R...](https://isitonrecall.com/recall/fda-device-z-2043-2025-medline-convenience-kits-containing-bd-insyte-autoguard-shielded-iv-catheters-22-ga-x-1-00-in-labele/) Medline Industries, LP. is issuing a recall for specific Medline kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN which was identified that during insertion of the Catheter, the needle is slow to retract or fails to retract. Class II Reported ongoing Distribution: US Nationwide distribution in the states of IN, KY, CA, MI, TX, WA. [Official source for Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. la...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2043-2025%22) May 23, 2025 FDA device enforcement ### [Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: IV START BOX, REF ACC010665](https://isitonrecall.com/recall/fda-device-z-2044-2025-medline-convenience-kits-containing-bd-insyte-autoguard-shielded-iv-catheters-22-ga-x-1-00-in-labele/) Medline Industries, LP. is issuing a recall for specific Medline kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN which was identified that during insertion of the Catheter, the needle is slow to retract or fails to retract. Class II Reported ongoing Distribution: US Nationwide distribution in the states of IN, KY, CA, MI, TX, WA. [Official source for Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. la...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2044-2025%22) May 23, 2025 FDA device enforcement ### [Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: RETINAL PACK-LF, REF DYNJ0151148B](https://isitonrecall.com/recall/fda-device-z-2045-2025-medline-convenience-kits-containing-bd-insyte-autoguard-shielded-iv-catheters-22-ga-x-1-00-in-labele/) Medline Industries, LP. is issuing a recall for specific Medline kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN which was identified that during insertion of the Catheter, the needle is slow to retract or fails to retract. Class II Reported ongoing Distribution: US Nationwide distribution in the states of IN, KY, CA, MI, TX, WA. [Official source for Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. la...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2045-2025%22) May 15, 2025 FDA device enforcement ### [Medline UMBILICAL TRAY W/3.5&5FR CATH, REF UVT1250](https://isitonrecall.com/recall/fda-device-z-1995-2025-medline-umbilical-tray-w-3-5-5fr-cath-ref-uvt1250/) There is a possible packaging defect impacting the outer Tyvec pouch that protects the sterile product. Class II Reported ongoing Distribution: US Nationwide distribution in the state of VA. [Official source for Medline UMBILICAL TRAY W/3.5&5FR CATH, REF UVT1250](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1995-2025%22) ## Reasons in these listed records - Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to the failure of the light to illuminate as intended. - Kits contain SureStep Foley Tray Systems recalled by BD that include incorrect product information insert sheets. If a mislabeled tray is used, patient risk ranges from minor injury to injury that requires medical intervention, such as infection or local/systemic allergic reac... - Specific lots of reprocessed electrophysiology catheters may contain small residual particulates. - Affected kits contain recalled Stryker Color Cuff Sterile Disposable Tourniquet Cuffs. Stryker Instruments initiated this recall due to a potential manufacturing defect in which the flange may detach from the bladder at the welded connection point. This detachment compromises ... These examples come from this result page and are not a ranking of every recall reason. ## Checking MEDLINE INDUSTRIES, LP - Northfield ### Is there a recall on medline industries, lp - northfield right now? This archive contains 822 records, including 809 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search MEDLINE INDUSTRIES, LP - Northfield](https://isitonrecall.com/check/?q=MEDLINE%20INDUSTRIES%2C%20LP%20-%20Northfield) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)