Notice names this product. Bayer Medical Care’s MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System is named in FDA Class II recall Z-3147-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Some devices may not have been properly sterilized due to a manufacturing sterilization issue. Identifying details: Catalog number: FLEXS-150-QFT; UDI-DI: 00616258022895; Affected material number: 87078825; Affected batch number: 8688750;. Units affected: 27800 kits (556 boxes). Status: Ongoing.
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System; Catalog number: FLEXS-150-QFT;
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
Some devices may not have been properly sterilized due to a manufacturing sterilization issue.
Company / brand: Bayer Medical Care recalls
Affected product: MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System recall status
Official ID Z-3147-2026 · Official record ↗
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Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.