FDA recall record

Access Vascular HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number recall — FDA Z-1605-2023

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…

Class IIclassification
Z-1605-2023official record ID
May 24, 2023report date

Recall record at a glance

Official recordZ-1605-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmAccess Vascular, Inc.
Report dateMay 24, 2023
Recall initiation dateMar 3, 2023
Quantity240 units
LocationBillerica, MA, United States

Official product description

HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004

Why the product was recalled

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.

Distribution information

US distribution to States of: FL, TN, TX.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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