--- title: "Access Vascular, Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Access Vascular, 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/access-vascular-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Access Vascular, Inc recall records **8** reported ongoing 8 records in this archive. Latest source date Aug 31, 2023. 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 31, 2023 FDA device enforcement ### [HydroPICC 5Fr Dual Lumen, 80cm guidewire - Basic Kit, Product Model Number 80002002](https://isitonrecall.com/recall/fda-device-z-0114-2024-hydropicc-5fr-dual-lumen-80cm-guidewire-basic-kit-product-model-number-80002002/) Specific lots of the Dual Lumen HydroPICC Kits were provided with the incorrect revision of the Instructions For Use (IFU) which do not include the following warnings statement: HydroPICC Dual Lumen Catheter is for adult use only. There is a potential risk ... Class II Reported ongoing Distribution: US Nationwide distribution in the states of IL, TX. [Official source for HydroPICC 5Fr Dual Lumen, 80cm guidewire - Basic Kit, Product Model Number 80002002](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0114-2024%22) Aug 31, 2023 FDA device enforcement ### [HydroPICC 5Fr Dual Lumen Maximal Barrier Kit, Product Model Number 80002004](https://isitonrecall.com/recall/fda-device-z-0115-2024-hydropicc-5fr-dual-lumen-maximal-barrier-kit-product-model-number-80002004/) Specific lots of the Dual Lumen HydroPICC Kits were provided with the incorrect revision of the Instructions For Use (IFU) which do not include the following warnings statement: HydroPICC Dual Lumen Catheter is for adult use only. There is a potential risk ... Class II Reported ongoing Distribution: US Nationwide distribution in the states of IL, TX. [Official source for HydroPICC 5Fr Dual Lumen Maximal Barrier Kit, Product Model Number 80002004](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0115-2024%22) Mar 3, 2023 FDA device enforcement ### [HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004](https://isitonrecall.com/recall/fda-device-z-1605-2023-hydropicc-4fr-single-lumen-catheter-maximal-barrier-kit-model-number-80001004/) The catheter packaged with specific lots of the HydroPICC Kits and HydroMID Kits have a shorter expiration date than what is listed on the outer kit package. Class II Reported ongoing Distribution: US distribution to States of: FL, TN, TX. [Official source for HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1605-2023%22) Dec 22, 2022 FDA device enforcement ### [HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short term access (](https://isitonrecall.com/recall/fda-device-z-1155-2023-hydromid-4fr-single-lumen-maximal-barrier-kit-indicated-for-short-term-access/) Product Mislabeled on the outer bag and inner kit Tyvek header bag Class II Reported ongoing Distribution: US Nationwide distribution in the states of FL, TX, WA. [Official source for HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short term access (](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1155-2023%22) Dec 22, 2022 FDA device enforcement ### [HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term access (](https://isitonrecall.com/recall/fda-device-z-1156-2023-hydromid-4fr-single-lumen-maximal-barrier-kit-indicated-for-short-term-access/) Label with the incorrect component listed on the inner kit Tyvek header bag Class II Reported ongoing Distribution: US Nationwide distribution in the states of CT, FL, NE, TN, TX, WA. [Official source for HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term access (](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1156-2023%22) Dec 16, 2022 FDA device enforcement ### [HydroMID 4Fr Single Lumen - Basic Kit, Model Number 80004002](https://isitonrecall.com/recall/fda-device-z-1129-2023-hydromid-4fr-single-lumen-basic-kit-model-number-80004002/) Select catheter lots were identified to be labeled with incorrect expiration date, where the catheters expire prior to the labeled expiration date of the kit. Class II Reported ongoing Distribution: US Nationwide distribution in the states of CT, IL, IN, MA, NE, TN, and TX. [Official source for HydroMID 4Fr Single Lumen - Basic Kit, Model Number 80004002](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1129-2023%22) Dec 16, 2022 FDA device enforcement ### [HydroPICC 4Fr Single Lumen, 80cm Guidewire - Basic Kit, Model Number 80001002](https://isitonrecall.com/recall/fda-device-z-1130-2023-hydropicc-4fr-single-lumen-80cm-guidewire-basic-kit-model-number-80001002/) Select catheter lots were identified to be labeled with incorrect expiration date, where the catheters expire prior to the labeled expiration date of the kit. Class II Reported ongoing Distribution: US Nationwide distribution in the states of CT, IL, IN, MA, NE, TN, and TX. [Official source for HydroPICC 4Fr Single Lumen, 80cm Guidewire - Basic Kit, Model Number 80001002](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1130-2023%22) Dec 16, 2022 FDA device enforcement ### [HydroPICC 4Fr Single Lumen, 130cm Guidewire - Basic Kit, Model Number 80001001](https://isitonrecall.com/recall/fda-device-z-1131-2023-hydropicc-4fr-single-lumen-130cm-guidewire-basic-kit-model-number-80001001/) Select catheter lots were identified to be labeled with incorrect expiration date, where the catheters expire prior to the labeled expiration date of the kit. Class II Reported ongoing Distribution: US Nationwide distribution in the states of CT, IL, IN, MA, NE, TN, and TX. [Official source for HydroPICC 4Fr Single Lumen, 130cm Guidewire - Basic Kit, Model Number 80001001](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1131-2023%22) ## Reasons in these listed records - Specific lots of the Dual Lumen HydroPICC Kits were provided with the incorrect revision of the Instructions For Use (IFU) which do not include the following warnings statement: HydroPICC Dual Lumen Catheter is for adult use only. There is a potential risk to health should the... - The catheter packaged with specific lots of the HydroPICC Kits and HydroMID Kits have a shorter expiration date than what is listed on the outer kit package. - Product Mislabeled on the outer bag and inner kit Tyvek header bag - Label with the incorrect component listed on the inner kit Tyvek header bag These examples come from this result page and are not a ranking of every recall reason. ## Checking Access Vascular, Inc ### Is there a recall on access vascular, inc right now? This archive contains 8 records, including 8 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 Access Vascular, Inc](https://isitonrecall.com/check/?q=Access%20Vascular%2C%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)