Access Vascular HydroPICC Kit: Incorrect Expiration Date Risk
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.
Lower-risk recall
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.
Contact the company
What happened, in plain English
Access Vascular is recalling HydroPICC 4Fr Single Lumen kits with model number 80001002 due to incorrect expiration dates on some catheters. Using these kits could lead to expired catheters that might not function properly or cause complications. Read more at govinfonow.com/recall/59099-access-vascular-hydropicc-kit-incorrect-expiration-date-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/59099-access-vascular-hydropicc-kit-incorrect-expiration-date-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1130-2023
Cite this page
“Access Vascular HydroPICC Kit: Incorrect Expiration Date Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/59099-access-vascular-hydropicc-kit-incorrect-expiration-date-risk. Based on FDA recall #Z-1130-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1130-2023%22&limit=1).
Why it’s dangerous
The catheters in these kits have incorrect expiration dates, meaning they may expire before the labeled date on the kit. This could lead to using expired catheters that might not function properly or cause complications during medical procedures.
Who’s affected
Healthcare providers using the HydroPICC 4Fr Single Lumen kits with model number 80001002 are likely affected. Patients receiving care through these kits may be at risk if the catheters expire prematurely.
How to tell if you have this one
Check for model number 80001002 on the HydroPICC 4Fr Single Lumen kits. Look for lot numbers 11389279 or 11391525 on the kit packaging.
- Brand
Access Vascular- Product
HydroPICC 4Fr Single Lumen, 80cm Guidewire - Basic Kit, Model Number 80001002- Category
Medical device
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
US Nationwide distribution in the states of CT, IL, IN, MA, NE, TN, and TX.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-1129-2023 | HydroMID 4Fr Single Lumen - Basic Kit, Model Number 80004002; UDI-DI: (01)00850030354006; Lot Number: 11428361, 11393260, 11395226 | 1,789 HydroMID devices |
| Z-1130-2023 | HydroPICC 4Fr Single Lumen, 80cm Guidewire - Basic Kit, Model Number 80001002; UDI-DI: (01)00862559000463; Lot Number: 11389279, 11391525 | N/A |
| Z-1131-2023 | HydroPICC 4Fr Single Lumen, 130cm Guidewire - Basic Kit, Model Number 80001001; UDI-DI: (01)00862559000456; Lot Number: 11398679, 11416178 | 302 HydroPICC devices |
What to do — step by step
Check Kit Expiration Dates
Verify the expiration date on the catheters matches the kit's labeled expiration date. If it does not, stop using the kit.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 7 states.
FDA distribution: “US Nationwide distribution in the states of CT, IL, IN, MA, NE, TN, and TX.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Connecticut, Illinois, Indiana, Massachusetts, Nebraska, Tennessee, Texas.
Recall timeline
FDA published this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Similar recalls
Latest medical device recalls
Keep exploring
Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1130-2023 (December 16, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1130-2023 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.