PMDA Class I Recall: Fresh Frozen Plasma-LR 'Nisseki' 240
クラスI回収 該当回収品目 新鮮凍結血漿-LR「日赤」240
Published: 2026-09-02 · Source: Pharmaceuticals and Medical Devices Agency (PMDA) — Safety Updates · Stage: Government Announcement · Area: Healthcare / Pharmaceuticals · Impact (preliminary): Medium · First detected by this dashboard: 2026-09-03
View the original Japanese source More Healthcare / Pharmaceuticals updates Search all updates in the dashboard
AI summary
Generated by AI from the Japanese source metadata. It is an unofficial monitoring aid, not legal advice, and may contain errors. The area, stage, and impact labels are preliminary keyword-based triage labels. Confirm every point in the original Japanese source.
Summary
The Pharmaceuticals and Medical Devices Agency (PMDA) has posted a safety notice concerning a Class I recall involving the product Fresh Frozen Plasma-LR 'Nisseki' 240. Based on the provided title, this is a government recall announcement listed among PMDA safety updates. Further details of the recall are not included in the provided metadata.
Business Impact
Organizations handling or administering this blood product may need to identify affected lots and assess whether any inventory or usage is involved. Healthcare and supply-chain stakeholders could be affected depending on the recall scope.
Recommended Action
Review the official PMDA recall notice at the provided source URL to confirm the affected product, lot details, and any recall instructions.