Drugs & medicalClass II

Access Vascular, Inc recalls 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.

Read the official notice →
Date
2023-02-22
Country
United States
Brand
Access Vascular
Product
HydroPICC 4Fr Single Lumen, 80cm Guidewire - Basic Kit, Model Number 80001002
Classification
Class II
Units
US Nationwide distribution in the states of CT, IL, IN, MA, NE, TN, and TX.
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Access Vascular recalls

  1. 2023-10-25
  2. US
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    Access Vascular, Inc recalls 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…

    FDA · DeviceAccess Vascular, IncUS Nationwide distribution in the states of IL, TX.Official notice →
  3. 2023-05-24
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    Access Vascular, Inc recalls 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.

    FDA · DeviceAccess Vascular, IncUS distribution to States of: FL, TN, TX.Official notice →
  5. 2023-03-01
  6. US
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    Access Vascular, Inc recalls HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term access (<30days) to the peripheral venous access system for…

    Label with the incorrect component listed on the inner kit Tyvek header bag

    FDA · DeviceAccess Vascular, IncUS Nationwide distribution in the states of CT, FL, NE, TN, TX, WA.Official notice →
  7. US
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    Access Vascular, Inc recalls HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short term access (<30days) to the peripheral venous access system for…

    Product Mislabeled on the outer bag and inner kit Tyvek header bag

    FDA · DeviceAccess Vascular, IncUS Nationwide distribution in the states of FL, TX, WA.Official notice →
  8. 2022-11-16
  9. US
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    Access Vascular, Inc. recalls Scalpel and StatLock included with HydroPICC Catheter Kit - PICC-142, Peripherally Inserted Central Catheter

    Scalpel and StatLock components packaged with specific lots of the HydroPICC catheter have a shorter expiration date than what is listed on the outer kit package.

    FDA · DeviceAccess Vascular, Inc.Domestic distribution to NC, RI, NJ, and IL. No foreign distribution.Official notice →
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