--- title: "Medline Industries, LP Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Medline Industries, LP 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/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Medline Industries, LP recall records **546** reported ongoing 549 records in this archive. Latest source date Aug 11, 2026. 3 published notices do not supply a closure status. 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 Aug 11, 2026 FDA device enforcement ### [Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET, Catalog Number: DYKMBNDL199A](https://isitonrecall.com/recall/fda-device-z-3121-2026-medline-convenience-kits-1-kit-anesthesia-l-d-a-line-set-catalog-number-dykmbndl199a/) The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus... Class I Reported ongoing Distribution: US Nationwide distribution. [Official source for Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET, Catalog Number: DYKMBNDL199A](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3121-2026%22) Aug 11, 2026 FDA device enforcement ### [Medline Convenience Kits: 1) OPEN HEART ADULT, Catalog Number: CDS840396Y; 2) FULL LINE ANEURYSM CDS, Catalog Number: CDS983672O; 3) NON STERILE CHEST TUBE REMOVAL, Catalog Numb...](https://isitonrecall.com/recall/fda-device-z-3122-2026-medline-convenience-kits-1-open-heart-adult-catalog-number-cds840396y-2-full-line-aneurysm-cds-catal/) The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus... Class I Reported ongoing Distribution: US Nationwide distribution. [Official source for Medline Convenience Kits: 1) OPEN HEART ADULT, Catalog Number: CDS840396Y; 2) FULL LINE ANEURYSM ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3122-2026%22) Aug 11, 2026 FDA device enforcement ### [Medline Convenience Kits: 1) PORT ACCESS KIT UNIV OF ALA, Catalog Number: DYKM1414; 2) ARTERIAL LINE ST JOES SYR PACK, Catalog Number: DYNJ38145F](https://isitonrecall.com/recall/fda-device-z-3123-2026-medline-convenience-kits-1-port-access-kit-univ-of-ala-catalog-number-dykm1414-2-arterial-line-st-jo/) The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus... Class I Reported ongoing Distribution: US Nationwide distribution. [Official source for Medline Convenience Kits: 1) PORT ACCESS KIT UNIV OF ALA, Catalog Number: DYKM1414; 2) ARTERIAL L...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3123-2026%22) Aug 11, 2026 FDA device enforcement ### [Medline Convenience Kits: 1) ACC010308A, Catalog Number: ACC010308A; 2) ACC010374A, Catalog Number: ACC010374A; 3) ACC010679, Catalog Number: ACC010679; 4) ACC010726A, Catalog N...](https://isitonrecall.com/recall/fda-device-z-3124-2026-medline-convenience-kits-1-acc010308a-catalog-number-acc010308a-2-acc010374a-catalog-number-acc01037/) The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus... Class I Reported ongoing Distribution: US Nationwide distribution. [Official source for Medline Convenience Kits: 1) ACC010308A, Catalog Number: ACC010308A; 2) ACC010374A, Catalog Numbe...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3124-2026%22) Aug 11, 2026 FDA device enforcement ### [Medline Convenience Kits: 1) DYKM1000B, Catalog Number: DYKM1000B; 2) DYKM2187A, Catalog Number: DYKM2187A](https://isitonrecall.com/recall/fda-device-z-3125-2026-medline-convenience-kits-1-dykm1000b-catalog-number-dykm1000b-2-dykm2187a-catalog-number-dykm2187a/) The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus... Class I Reported ongoing Distribution: US Nationwide distribution. [Official source for Medline Convenience Kits: 1) DYKM1000B, Catalog Number: DYKM1000B; 2) DYKM2187A, Catalog Number: ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3125-2026%22) Aug 11, 2026 FDA device enforcement ### [Medline Convenience Kits: 1) DYNDH1193, Catalog Number: DYNDH1193; 2) DYNDH1487A, Catalog Number: DYNDH1487A](https://isitonrecall.com/recall/fda-device-z-3126-2026-medline-convenience-kits-1-dyndh1193-catalog-number-dyndh1193-2-dyndh1487a-catalog-number-dyndh1487a/) The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus... Class I Reported ongoing Distribution: US Nationwide distribution. [Official source for Medline Convenience Kits: 1) DYNDH1193, Catalog Number: DYNDH1193; 2) DYNDH1487A, Catalog Number:...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3126-2026%22) Aug 11, 2026 FDA device enforcement ### [Medline Convenience Kits: 1) DYNDB3086D, Catalog Number: DYNDB3086D; 2) DYNDB3100, Catalog Number: DYNDB3100; 3) DYNDH1619A, Catalog Number: DYNDH1619A; 4) DYNDH1620A, Catalog N...](https://isitonrecall.com/recall/fda-device-z-3127-2026-medline-convenience-kits-1-dyndb3086d-catalog-number-dyndb3086d-2-dyndb3100-catalog-number-dyndb3100/) The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus... Class I Reported ongoing Distribution: US Nationwide distribution. [Official source for Medline Convenience Kits: 1) DYNDB3086D, Catalog Number: DYNDB3086D; 2) DYNDB3100, Catalog Number...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3127-2026%22) Aug 6, 2026 FDA company announcement ### [Medline, Teleflex: Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits](https://isitonrecall.com/recall/fdapress-1c8bd6cdabe7c66e-medline-teleflex-hudson-rci-neonatal-infant-heated-wire-breathing-circuits/) Due to heated wire connector (pigtail) at the Neptune humidifier may exhibit discoloration, melting, smoke, burning odor, or other signs of localized thermal damage Not supplied Published notice; closure not supplied Distribution: Not supplied [Official source for Medline, Teleflex: Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/medline-industries-lp-issues-nationwide-recall-hudson-rci-neonatalinfant-heated-wire-breathing) Jul 31, 2026 FDA device enforcement ### [Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A](https://isitonrecall.com/recall/fda-device-z-3207-2026-convenience-kits-anesthesia-pain-pk-league-dynj67925a/) Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used. Class II Reported ongoing Distribution: US Nationwide distribution in states of Arkansas, Florida, North Carolina, Maryland, and Texas. [Official source for Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3207-2026%22) Jul 31, 2026 FDA device enforcement ### [Convenience kits MINOR PACK DYNJ58421A SPRINGHILL MINOR PACK DYNJ40734F](https://isitonrecall.com/recall/fda-device-z-3208-2026-convenience-kits-minor-pack-dynj58421a-springhill-minor-pack-dynj40734f/) Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used. Class II Reported ongoing Distribution: US Nationwide distribution in states of Arkansas, Florida, North Carolina, Maryland, and Texas. [Official source for Convenience kits MINOR PACK DYNJ58421A SPRINGHILL MINOR PACK DYNJ40734F](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3208-2026%22) Jul 31, 2026 FDA device enforcement ### [Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A](https://isitonrecall.com/recall/fda-device-z-3209-2026-convenience-kits-myringotomy-pack-lf-dynj59097a/) Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used. Class II Reported ongoing Distribution: US Nationwide distribution in states of Arkansas, Florida, North Carolina, Maryland, and Texas. [Official source for Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3209-2026%22) Jul 31, 2026 FDA device enforcement ### [Convenience kits CATARACT PACK DYNJ59881A](https://isitonrecall.com/recall/fda-device-z-3210-2026-convenience-kits-cataract-pack-dynj59881a/) Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used. Class II Reported ongoing Distribution: US Nationwide distribution in states of Arkansas, Florida, North Carolina, Maryland, and Texas. [Official source for Convenience kits CATARACT PACK DYNJ59881A](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3210-2026%22) Jul 23, 2026 FDA device enforcement ### [Medline Convenience Kit: OPEN HEART A PACK, Product Number DYNJ43008N](https://isitonrecall.com/recall/fda-device-z-3137-2026-medline-convenience-kit-open-heart-a-pack-product-number-dynj43008n/) The kits contain a Retrograde Coronary Sinus Perfusion (RCSP) cannulae that has the potential for a sterile barrier breach. Sterility of the product cannot be assured. If a compromised pouch seal is not identified prior to use and the cannula is used, there... Class II Reported ongoing Distribution: US Nationwide distribution in the state of CA. [Official source for Medline Convenience Kit: OPEN HEART A PACK, Product Number DYNJ43008N](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3137-2026%22) Jul 20, 2026 FDA device enforcement ### [Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PAIN PRE OP KIT DYKS1476A](https://isitonrecall.com/recall/fda-device-z-3067-2026-medline-convenience-kits-containing-bd-chloraprep-clear-1ml-applicators-pain-pre-op-kit-dyks1476a/) Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to loc... Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PAIN PRE OP KIT DYKS1476A](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3067-2026%22) Jul 20, 2026 FDA device enforcement ### [Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators OPEN HEART CDS983348AA CDS983348AB](https://isitonrecall.com/recall/fda-device-z-3068-2026-medline-convenience-kits-containing-bd-chloraprep-clear-1ml-applicators-open-heart-cds983348aa-cds98/) Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to loc... Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators OPEN HEART CDS983348AA ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3068-2026%22) Jul 20, 2026 FDA device enforcement ### [Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BASIN PACK-LF DYNJ42828B EYE BASIN TRAY-LF DYNJ42832B](https://isitonrecall.com/recall/fda-device-z-3069-2026-medline-convenience-kits-containing-bd-chloraprep-clear-1ml-applicators-basin-pack-lf-dynj42828b-eye/) Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to loc... Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BASIN PACK-LF DYNJ42828...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3069-2026%22) Jul 20, 2026 FDA device enforcement ### [Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULTURE PINK PERIPHERAL DYNDV1875 BOTTOM DRAWER ACC010972 DRAWER #4 ACC010479A DRAWER 2 ACC010690...](https://isitonrecall.com/recall/fda-device-z-3070-2026-medline-convenience-kits-containing-bd-chloraprep-clear-1ml-applicators-blood-culture-pink-periphera/) Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to loc... Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULTURE PINK PERI...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3070-2026%22) Jul 20, 2026 FDA device enforcement ### [Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators IV START KIT LAB DRAW-SH CDS860014Q IV START KIT DYKM1000B IV START KIT LAB DRAW-SH CDS860014P ULTRASOU...](https://isitonrecall.com/recall/fda-device-z-3071-2026-medline-convenience-kits-containing-bd-chloraprep-clear-1ml-applicators-iv-start-kit-lab-draw-sh-cds/) Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to loc... Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators IV START KIT LAB DRAW-S...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3071-2026%22) Jul 20, 2026 FDA device enforcement ### [Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULTURE KIT 2 W/CONNECT DYNDH1487A](https://isitonrecall.com/recall/fda-device-z-3072-2026-medline-convenience-kits-containing-bd-chloraprep-clear-1ml-applicators-blood-culture-kit-2-w-connec/) Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to loc... Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULTURE KIT 2 W/C...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3072-2026%22) Jul 20, 2026 FDA device enforcement ### [Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ADULT BLOOD CULTURE KIT DYNDH1444D BLOOD CULTR KT DIVRSN DEVICE DYNDH1866 BLOOD CULTURE KIT DYNDH1462B ...](https://isitonrecall.com/recall/fda-device-z-3073-2026-medline-convenience-kits-containing-bd-chloraprep-clear-1ml-applicators-adult-blood-culture-kit-dynd/) Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to loc... Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ADULT BLOOD CULTURE KIT...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3073-2026%22) ## Reasons in these listed records - The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may ... - Due to heated wire connector (pigtail) at the Neptune humidifier may exhibit discoloration, melting, smoke, burning odor, or other signs of localized thermal damage - Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used. - The kits contain a Retrograde Coronary Sinus Perfusion (RCSP) cannulae that has the potential for a sterile barrier breach. Sterility of the product cannot be assured. If a compromised pouch seal is not identified prior to use and the cannula is used, there is a potential risk... These examples come from this result page and are not a ranking of every recall reason. ## Checking Medline Industries, LP ### Is there a recall on medline industries, lp right now? This archive contains 549 records, including 546 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](https://isitonrecall.com/check/?q=Medline%20Industries%2C%20LP) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)