FDA Device Intelligence
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Injector, Contrast Medium, Automatic

FDA product code IZQ · Class 2 · Cardiovascular

142
Registered devices
576
Adverse events
3
Recalls
23
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2011-10-11Mallinckrodt IncSyringes packaged and labeled as the Illumena 150mL Linden Luer Syringe with Handi-Fil Straw, product 900103, contained the Illumena 150mL Syringe with Handi-Fi
2011-05-20Mallinckrodt IncSyringes packaged and labeled as the Illumena 150mL Linden Luer Syringe with Handi-Fil Straw, product 900103, contained the Illumena150mL Syringe with Handi-Fil
2008-04-07Mallinckrodt IncScrews can begin to loosen and shear off to the point of the J-Bow falling from the suspension system. This may cause injury to patients or hospital staff.

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