HydroMID 4Fr Single Lumen - Basic Kit, Model Number 80004002
Reported: February 22, 2023 Initiated: December 16, 2022 #Z-1129-2023
Product Description
HydroMID 4Fr Single Lumen - Basic Kit, Model Number 80004002
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
- 1,789 HydroMID 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? ▼
HydroMID 4Fr Single Lumen - Basic Kit, Model Number 80004002. Recalled by Access Vascular, Inc. Units affected: 1,789 HydroMID 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-1129-2023.
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