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Intravenous Extension Tubing Set

FDA product code OJA · Class 2 · General Hospital

540
Registered devices
39
Adverse events
4
Recalls
1
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-07-14Cardinal Health 200, LLCCardinal Health was recently informed of a medical device recall from MEDICOM concerning the Ritmed Neurological Sponges. The recall is being issued due to unex
2025-06-05Merit Medical Systems, Inc.High pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line. Use of the affec
2024-06-11Merit Medical Systems, Inc.Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have bee
2024-06-11Merit Medical Systems, Inc.Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have bee

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.