Class II

Medical Device Recall: MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System; Catalog number: FLEXS-150-QFT;

Bayer Medical Care, Inc. · July 31, 2026

Reason for Recall

Some devices may not have been properly sterilized due to a manufacturing sterilization issue.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

27800 kits (556 boxes)

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3147-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Bayer Medical Care, Inc. Medical Device Recall: MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System; Catalog number: FLEXS-150-QFT; | SafeCheck