--- title: "American Contract Systems, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search American Contract Systems, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/american-contract-systems-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # American Contract Systems, Inc. recall records **193** reported ongoing 194 records in this archive. Latest source date Jun 29, 2026. 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 Jun 29, 2026 FDA device enforcement ### [American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AM](https://isitonrecall.com/recall/fda-device-z-3000-2026-american-contract-system-convenience-kit-cv-b-pack-model-catalog-number-tncb10am/) The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representative samples did not meet applicable performance specifications. Class II Reported ongoing Distribution: US Nationwide distribution in the states of IA, OH. [Official source for American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AM](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3000-2026%22) Jun 29, 2026 FDA device enforcement ### [American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AN](https://isitonrecall.com/recall/fda-device-z-3001-2026-american-contract-system-convenience-kit-cv-b-pack-model-catalog-number-tncb10an/) The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representative samples did not meet applicable performance specifications. Class II Reported ongoing Distribution: US Nationwide distribution in the states of IA, OH. [Official source for American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AN](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3001-2026%22) Jun 29, 2026 FDA device enforcement ### [American Contract System Convenience Kits, CV B PACK, Model/Catalog Number: TNCB10AP](https://isitonrecall.com/recall/fda-device-z-3002-2026-american-contract-system-convenience-kits-cv-b-pack-model-catalog-number-tncb10ap/) The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representative samples did not meet applicable performance specifications. Class II Reported ongoing Distribution: US Nationwide distribution in the states of IA, OH. [Official source for American Contract System Convenience Kits, CV B PACK, Model/Catalog Number: TNCB10AP](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3002-2026%22) Jun 29, 2026 FDA device enforcement ### [American Contract System Convenience Kit, D & C PACK, Model/Catalog Number: LLPD90H](https://isitonrecall.com/recall/fda-device-z-3003-2026-american-contract-system-convenience-kit-d-c-pack-model-catalog-number-llpd90h/) The Convenience Kits contain Medline's Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representative samples did not meet applicable performance specifications. Class II Reported ongoing Distribution: US Nationwide distribution in the states of IA, OH. [Official source for American Contract System Convenience Kit, D & C PACK, Model/Catalog Number: LLPD90H](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3003-2026%22) May 19, 2026 FDA device enforcement ### [American Contract Systems medical procedure kits and trays labeled as: 1) CRANI PACK - 208400, Model Item Number UDCP57AI; 2) SPINE PACK, Model Item Number HSLM53AC; 3) CRANIAL ...](https://isitonrecall.com/recall/fda-device-z-2989-2026-american-contract-systems-medical-procedure-kits-and-trays-labeled-as-1-crani-pack-208400-model-item/) The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the prod... Class II Reported ongoing Distribution: US distribution to states of: MN, MO, IA [Official source for American Contract Systems medical procedure kits and trays labeled as: 1) CRANI PACK - 208400, Mo...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2989-2026%22) May 19, 2026 FDA device enforcement ### [American Contract Systems medical procedure kits and trays labeled as: 1) ANTERIOR CERVICAL PACK - 205988, Model Item Number MHAC65AH; 2) SPINE PACK - 206013, Model Item Number ...](https://isitonrecall.com/recall/fda-device-z-2990-2026-american-contract-systems-medical-procedure-kits-and-trays-labeled-as-1-anterior-cervical-pack-20598/) The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the prod... Class II Reported ongoing Distribution: US distribution to states of: MN, MO, IA [Official source for American Contract Systems medical procedure kits and trays labeled as: 1) ANTERIOR CERVICAL PACK ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2990-2026%22) Mar 19, 2026 FDA device enforcement ### [Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Model numbers ANCA80AP ANCA80AQ](https://isitonrecall.com/recall/fda-device-z-1981-2026-convenience-kits-containing-medline-namic-angiographic-control-syringes-with-rotating-adaptor-corona/) Impacted kits contain syringes recalled by Medline Industries. Syringe rotating adaptor may unwind during use, which may result in a loose connection or full disconnection between the syringe and manifold. Potential risk for biohazard exposure, blood loss, ... Class I Reported ongoing Distribution: US distribution to MN. No OUS distribution. [Official source for Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor COR...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1981-2026%22) Sep 4, 2025 FDA device enforcement ### [Basic Biopsy Tray, Item Number NMBP44L](https://isitonrecall.com/recall/fda-device-z-0170-2026-basic-biopsy-tray-item-number-nmbp44l/) Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, pro... Class II Reported ongoing Distribution: US Nationwide distribution in the states of SD, IA, MN, WA, IL. [Official source for Basic Biopsy Tray, Item Number NMBP44L](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0170-2026%22) Sep 4, 2025 FDA device enforcement ### [Basic Biopsy Tray; Item Number/Description: AKRB26D ROBOTIC, AMGL09AA GENERAL LAPAROSCOPY, ANLC35AD LAP CHOLE PACK - 205956, ANLP25AJ LAPROSCOPY PACK - 205958, FYLA38E LAPCHOLAP...](https://isitonrecall.com/recall/fda-device-z-0171-2026-basic-biopsy-tray-item-number-description-akrb26d-robotic-amgl09aa-general-laparoscopy-anlc35ad-lap/) Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, pro... Class II Reported ongoing Distribution: US Nationwide distribution in the states of SD, IA, MN, WA, IL. [Official source for Basic Biopsy Tray; Item Number/Description: AKRB26D ROBOTIC, AMGL09AA GENERAL LAPAROSCOPY, ANLC35...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0171-2026%22) Sep 4, 2025 FDA device enforcement ### [Medical convenience kits Item number/ Product description AKGN82E GENERAL AMCB08Y CHEST BREAST PACK ANBP10AC BASIC PACK - 205939 ANIR77AM INTERVENTIONAL RADIOLOGY PACK - 205953 ...](https://isitonrecall.com/recall/fda-device-z-0172-2026-medical-convenience-kits-item-number-product-description-akgn82e-general-amcb08y-chest-breast-pack-a/) Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, pro... Class II Reported ongoing Distribution: US Nationwide distribution in the states of SD, IA, MN, WA, IL. [Official source for Medical convenience kits Item number/ Product description AKGN82E GENERAL AMCB08Y CHEST BREAST PA...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0172-2026%22) Sep 4, 2025 FDA device enforcement ### [Medical convenience kits Item number/ Product description AHLD15X LABOR DELIVERY PACK - 213387 AKDV96B VAGINAL DELIVERY AKDV96B VAGINAL DELIVERY EVBH28D BIRTHING ROOM PACK UPVD0...](https://isitonrecall.com/recall/fda-device-z-0173-2026-medical-convenience-kits-item-number-product-description-ahld15x-labor-delivery-pack-213387-akdv96b/) Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, pro... Class II Reported ongoing Distribution: US Nationwide distribution in the states of SD, IA, MN, WA, IL. [Official source for Medical convenience kits Item number/ Product description AHLD15X LABOR DELIVERY PACK - 213387 AK...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0173-2026%22) Sep 4, 2025 FDA device enforcement ### [Medical convenience kits Item Number/Description BUCY78E CYSTO PACK CMCP10X CYSTO PACK - 205972 IHCY10Y CYSTO PACK MHCY35AE CYSTO PACK- 212487 PLBY52E CYSTO PACK UDCY31Z CYSTO P...](https://isitonrecall.com/recall/fda-device-z-0174-2026-medical-convenience-kits-item-number-description-bucy78e-cysto-pack-cmcp10x-cysto-pack-205972-ihcy10/) Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, pro... Class II Reported ongoing Distribution: US Nationwide distribution in the states of SD, IA, MN, WA, IL. [Official source for Medical convenience kits Item Number/Description BUCY78E CYSTO PACK CMCP10X CYSTO PACK - 205972 I...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0174-2026%22) Sep 4, 2025 FDA device enforcement ### [Medical convenience kits Item Number/Description EVLH67F LEFT HEART CATH PACK FDCL22R CATH LAB ANGIO IHCC03X CATH CARDIAC PACK TNCC02AD CARDIAC CATH TRINITY UICC27AG CARDIAC CAT...](https://isitonrecall.com/recall/fda-device-z-0175-2026-medical-convenience-kits-item-number-description-evlh67f-left-heart-cath-pack-fdcl22r-cath-lab-angio/) Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, pro... Class II Reported ongoing Distribution: US Nationwide distribution in the states of SD, IA, MN, WA, IL. [Official source for Medical convenience kits Item Number/Description EVLH67F LEFT HEART CATH PACK FDCL22R CATH LAB AN...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0175-2026%22) Sep 4, 2025 FDA device enforcement ### [Medical convenience kits Item Number/Description ANCV78BC HEART PACK - 205947 HGCV05K CV SET UP PACK MHPP97AR PACEMAKER PACK- 206010 UDBH37AW BASIC HEART PACK - 206044 UHPP82AH ...](https://isitonrecall.com/recall/fda-device-z-0176-2026-medical-convenience-kits-item-number-description-ancv78bc-heart-pack-205947-hgcv05k-cv-set-up-pack-m/) Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, pro... Class II Reported ongoing Distribution: US Nationwide distribution in the states of SD, IA, MN, WA, IL. [Official source for Medical convenience kits Item Number/Description ANCV78BC HEART PACK - 205947 HGCV05K CV SET UP P...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0176-2026%22) Sep 4, 2025 FDA device enforcement ### [Medical convenience kits Item Number/Description UICL44P ADULT CENTRAL LINE INSERTION SUPPLY KIT UICL44R ADULT CENTRAL LINE INSERTION SUPPLY KIT](https://isitonrecall.com/recall/fda-device-z-0177-2026-medical-convenience-kits-item-number-description-uicl44p-adult-central-line-insertion-supply-kit-uic/) Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, pro... Class II Reported ongoing Distribution: US Nationwide distribution in the states of SD, IA, MN, WA, IL. [Official source for Medical convenience kits Item Number/Description UICL44P ADULT CENTRAL LINE INSERTION SUPPLY KIT ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0177-2026%22) Sep 4, 2025 FDA device enforcement ### [Medical convenience kits Item Number/Description RCEN25B ENT SDSC 0246972 RCHN27D HEAD AND NECK RCH 0246951](https://isitonrecall.com/recall/fda-device-z-0178-2026-medical-convenience-kits-item-number-description-rcen25b-ent-sdsc-0246972-rchn27d-head-and-neck-rch/) Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, pro... Class II Reported ongoing Distribution: US Nationwide distribution in the states of SD, IA, MN, WA, IL. [Official source for Medical convenience kits Item Number/Description RCEN25B ENT SDSC 0246972 RCHN27D HEAD AND NECK R...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0178-2026%22) Sep 4, 2025 FDA device enforcement ### [Medical convenience kits Item Number/Description RCGY52D GYN LAPAROSCOPY SPH 0246965 UIGN82M GYN (PS 907645) UIHY16AE ASC HYSTEROSCOPY PACK (PS 020634)](https://isitonrecall.com/recall/fda-device-z-0179-2026-medical-convenience-kits-item-number-description-rcgy52d-gyn-laparoscopy-sph-0246965-uign82m-gyn-ps/) Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, pro... Class II Reported ongoing Distribution: US Nationwide distribution in the states of SD, IA, MN, WA, IL. [Official source for Medical convenience kits Item Number/Description RCGY52D GYN LAPAROSCOPY SPH 0246965 UIGN82M GYN ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0179-2026%22) Sep 4, 2025 FDA device enforcement ### [Medical convenience kits Item Number/Description HSAN63N ANGIO PACK IHAN02W ANGIOGRAPHY PACK MHCA98AK CORONARY ANGIO PACK- 205991 RCAN45C ANGIO CUSTOM RCH UDCO10F CVL CORONARY P...](https://isitonrecall.com/recall/fda-device-z-0180-2026-medical-convenience-kits-item-number-description-hsan63n-angio-pack-ihan02w-angiography-pack-mhca98a/) Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, pro... Class II Reported ongoing Distribution: US Nationwide distribution in the states of SD, IA, MN, WA, IL. [Official source for Medical convenience kits Item Number/Description HSAN63N ANGIO PACK IHAN02W ANGIOGRAPHY PACK MHCA...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0180-2026%22) Sep 4, 2025 FDA device enforcement ### [Medical convenience kits Item Number/Description FHCP08Y C SECTION PK HICS50I C-SECTION PACK HSCB90B C-SECTION BASIN PACK](https://isitonrecall.com/recall/fda-device-z-0181-2026-medical-convenience-kits-item-number-description-fhcp08y-c-section-pk-hics50i-c-section-pack-hscb90b/) Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, pro... Class II Reported ongoing Distribution: US Nationwide distribution in the states of SD, IA, MN, WA, IL. [Official source for Medical convenience kits Item Number/Description FHCP08Y C SECTION PK HICS50I C-SECTION PACK HSCB...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0181-2026%22) Sep 4, 2025 FDA device enforcement ### [Medical convenience kits Item Number/Description LKRA40G RADIOLOGY PACK](https://isitonrecall.com/recall/fda-device-z-0182-2026-medical-convenience-kits-item-number-description-lkra40g-radiology-pack/) Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, pro... Class II Reported ongoing Distribution: US Nationwide distribution in the states of SD, IA, MN, WA, IL. [Official source for Medical convenience kits Item Number/Description LKRA40G RADIOLOGY PACK](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0182-2026%22) ## Reasons in these listed records - The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representative samples did not meet applicable performance specifications. - The Convenience Kits contain Medline's Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representative samples did not meet applicable performance specifications. - The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products. - Impacted kits contain syringes recalled by Medline Industries. Syringe rotating adaptor may unwind during use, which may result in a loose connection or full disconnection between the syringe and manifold. Potential risk for biohazard exposure, blood loss, infection, or air em... These examples come from this result page and are not a ranking of every recall reason. ## Checking American Contract Systems, Inc. ### Is there a recall on american contract systems, inc. right now? This archive contains 194 records, including 193 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 American Contract Systems, Inc.](https://isitonrecall.com/check/?q=American%20Contract%20Systems%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)