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Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Recalled — do not eat Announced September 3, 2026 - Ongoing - Not yet classified

Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial from American Regent, Inc. was recalled on September 3, 2026. Reason for the recall: Presence of particulate matter and lack of sterility assurance. The affected Lot Numbers 25128L1C0, 25280L1C0, and 26108L1C0 were distributed nationwide, in the United States. As of the latest federal update, the FDA classification is Not yet classified and the recall status is ongoing. Do not consume - Check details.

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Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial
Photo: FDA recall notice

Recalled products

ProductLot / codeClassRecall #
Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial---

Where it was sold

The affected Lot Numbers 25128L1C0, 25280L1C0, and 26108L1C0 were distributed nationwide, in the United States.

Sold nationwide.

Timeline

Announced (first public date)
September 3, 2026
Recall started by the firm
September 3, 2026

Official source: FDA recall notice

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