Access Vascular, Inc recalls
Every recall we track for Access Vascular, Inc — 9 in all, from 2021–2023 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Access Vascular, Inc peaked in 2022 (5); 9 since 2017.
All FDA recall records for Access Vascular, Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 5 | 0 | 5 |
| 2023 | 0 | 0 | 3 | 0 | 3 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Access Vascular, Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Access Vascular, Inc recalls
6 shown- Lower riskMedical device
Access Vascular, Inc recalls HydroPICC 5Fr Dual Lumen, 80cm guidewire - Basic Kit, Product Model Number 80002002
Access Vascular recalls HydroPICC 5Fr Dual Lumen kits with incorrect instructions that omit adult use warnings. This could risk harm if used in inadequately sized vessels. No injuries reported.
Access VascularAug 31, 2023 - Lower riskMedical device
Access Vascular, Inc recalls HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004
Access Vascular recalls HydroPICC 4Fr Single Lumen Catheter kits with shorter expiration dates than listed on packaging. Affected lots may expire sooner than expected.
Access VascularMar 3, 2023 - Lower riskMedical device
Access Vascular, Inc recalls HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term access (<30days) to the peripheral venous access
Access Vascular recalls HydroMID 4Fr Single Lumen Maximal Barrier Kit for incorrect label on inner Tyvek bag. This may cause confusion during IV therapy. Check product details to see if affected.
Access VascularDec 22, 2022 - Lower riskMedical device
Access Vascular, Inc recalls HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short term access (<30days) to the peripheral venous
Access Vascular recalls HydroMID 4Fr Single Lumen Maximal Barrier Kit due to mislabeling on outer and inner bags. This may lead to incorrect product use in IV therapy. No remedy specified in recall notice.
Access VascularDec 22, 2022 - Lower riskMedical device
Access Vascular, Inc recalls HydroPICC 4Fr Single Lumen, 80cm Guidewire - Basic Kit, Model Number 80001002
Access Vascular recalls HydroPICC 4Fr Single Lumen kits with incorrect expiration dates that could expire before the labeled date, posing a risk of using expired catheters.
Access VascularDec 16, 2022 - Lower riskMedical device
Access Vascular, Inc. recalls Scalpel and StatLock included with HydroPICC Catheter Kit - PICC-142, Peripherally Inserted Central Catheter
Access Vascular recalls HydroPICC Catheter Kit (PICC-142) with Scalpels and StatLocks that have shorter expiration dates than listed on the outer package. Consumers should check kit lot numbers and expiration dates.
Access VascularFeb 24, 2021
Access Vascular, Inc recall questions
How many recalls has Access Vascular, Inc had?
9 recalls from Access Vascular, Inc are on record with U.S. safety agencies, from 2021–2023.
What is the most recent Access Vascular, Inc recall?
Access Vascular, Inc recalls HydroPICC 5Fr Dual Lumen, 80cm guidewire - Basic Kit, Product Model Number 80002002, dated Aug 31, 2023. Every Access Vascular, Inc recall is listed on this page, newest first.
What should I do if I have a recalled Access Vascular, Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Access Vascular, Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.