Baxter CLEARLINK System, Non-DEHP Solution Set with DUO-VENT Spike, Product Code 2R8403. An in-line injection site.
Reported: September 21, 2022 Initiated: August 9, 2022 #Z-1653-2022
Product Description
Baxter CLEARLINK System, Non-DEHP Solution Set with DUO-VENT Spike, Product Code 2R8403. An in-line injection site.
Reason for Recall
Firm noted an increase in customer reports of leaks.
Details
- Recalling Firm
- Baxter Healthcare Corporation
- Units Affected
- 511,728 units
- Distribution
- US Nationwide Distribution
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
Baxter CLEARLINK System, Non-DEHP Solution Set with DUO-VENT Spike, Product Code 2R8403. An in-line injection site.. Recalled by Baxter Healthcare Corporation. Units affected: 511,728 units.
Why was this product recalled? ▼
Firm noted an increase in customer reports of leaks.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 21, 2022. Severity: Critical. Recall number: Z-1653-2022.
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