HydroPICC 4Fr Single Lumen, 130cm Guidewire - Basic Kit, Model Number 80001001
Reported: February 22, 2023 Initiated: December 16, 2022 #Z-1131-2023
Product Description
HydroPICC 4Fr Single Lumen, 130cm Guidewire - Basic Kit, Model Number 80001001
Reason for 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.
Details
- Recalling Firm
- Access Vascular, Inc
- Units Affected
- 302 HydroPICC devices
- Distribution
- US Nationwide distribution in the states of CT, IL, IN, MA, NE, TN, and TX.
- Location
- Billerica, MA
Frequently Asked Questions
What product was recalled? ▼
HydroPICC 4Fr Single Lumen, 130cm Guidewire - Basic Kit, Model Number 80001001. Recalled by Access Vascular, Inc. Units affected: 302 HydroPICC devices.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 22, 2023. Severity: Moderate. Recall number: Z-1131-2023.
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