Device recall: MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System; Catalog number: FLEXS-150-QFT;
Official structured record identifier: 99698.
Publisher
USA
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- Publisher
- openFDA Device Recalls
- Region
- USA
- Scope
- Regulatory
- Published
- September 23, 2026
- Language
- EN
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Official structured record identifier: 99698.
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Source: openFDA Device Recalls
Scope: Regulatory
Evidence: Tier 1 · Regulatory source
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