FDA-Device2024-03-20Class II
CLEARLINK Non-DEHP Solution Set Luer Lock Adapter, Product Code 2R8401
Hazard
Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Clearlink Non-DEHP solution set listed below due to potential leaks originating from the drip chamber.
Sold states
US Nationwide distribution.
Affected count
26,592 units
Manufactured in
1 Baxter Pkwy, N/A, Deerfield, IL, United States
Products
CLEARLINK Non-DEHP Solution Set Luer Lock Adapter, Product Code 2R8401
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1291-2024More Baxter Healthcare Corporation recalls
- FDA-Device2026-07-08Hillrom VOLARA System P.CIRCUIT KIT AC recalled for nebulizer cup leakage risk
- FDA-Device2026-07-08Baxter operating table head positioning adapter recalled for loosening risk
- FDA-Device2026-07-08Hillrom VOLARA System P.CIRCUIT 5KIT AC recalled for nebulizer cup leakage risk
- FDA-Device2026-07-08Hillrom VOLARA System P.CIRCUIT KIT recalled for nebulizer cup leakage risk
- FDA-Device2026-07-08Hillrom Volara P.Circuit 5Kit breathing device recalled for nebulizer cup leakage risk
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