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Policy version 2026-07-21, effective July 21, 2026.
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Based on the official records currently available to Public Health Trace, no recalls naming Adamis Pharmaceuticals Corporation are currently shown as ongoing. The 2 records below are historical recall records.
Public Health Trace has 2 recalls naming Adamis Pharmaceuticals Corporation as the recalling firm, republished from official FDA and USDA sources.
Recall history - 2 terminated records
Recalls by year
A bar chart of the number of recalls naming this company by year.
FDA RecallTerminatedTerminated: February 8, 2023Historical recordClass I
SYMJEPI (epinephrine injection, USP) 0.15 mg (0.15 mg/0.3 mL), Two Pre-Filled Single-Dose Syringes per carton, Rx Only, Manufactured for Adamis Pharmaceuticals Corp.; San Diego, CA 92130; Distributed by USWM, LLC., Louisville, KY 40241, Made in Belgium, NDC 78670-131-02.
by Adamis Pharmaceuticals Corporation
Reason
Defective Delivery System: Potential clogging of the needle preventing the dispensing of epinephrine.
FDA RecallTerminatedTerminated: February 8, 2023Historical recordClass I
SYMJEPI (epinephrine injection, USP) 0.3 mg, (0.3 mg/0.3 mL), Two Pre-Filled Single-Dose Syringes per carton, Rx Only, Manufactured for Adamis Pharmaceuticals Corp.; San Diego, CA 92130; Distributed by USWM, LLC., Louisville, KY 40241, Made in Belgium, NDC 78670-130-02
by Adamis Pharmaceuticals Corporation
Reason
Defective Delivery System: Potential clogging of the needle preventing the dispensing of epinephrine.
Some FDA recall records on this page come from FDA's Enforcement Report database.
Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
This page lists recalls that name Adamis Pharmaceuticals Corporation as the recalling firm in the official source notice. It is
not a safety rating, ranking, or statement that the company acted negligently.
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