HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004
Reported: May 24, 2023 Initiated: March 3, 2023 #Z-1605-2023
Product Description
HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004
Reason for Recall
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.
Details
- Recalling Firm
- Access Vascular, Inc
- Units Affected
- 240 units
- Distribution
- US distribution to States of: FL, TN, TX.
- Location
- Billerica, MA
Frequently Asked Questions
What product was recalled? ▼
HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004. Recalled by Access Vascular, Inc. Units affected: 240 units.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 24, 2023. Severity: Moderate. Recall number: Z-1605-2023.
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