Adamis recalls SYMJEPI epinephrine injections due to potential needle clogging. This could prevent proper epinephrine delivery during emergencies. Check your product details and contact Adamis for instructions.
Defective Delivery System: Potential clogging of the needle preventing the dispensing of epinephrine.
Adamis is recalling SYMJEPI epinephrine injections that may clog the needle, preventing proper delivery of epinephrine during emergencies. This is a serious hazard for people who need the injection for allergic reactions or anaphylaxis.
The syringes may clog the needle, which could prevent epinephrine from being delivered properly during an emergency. This is dangerous because epinephrine is critical for treating severe allergic reactions.
People with prescriptions for SYMJEPI epinephrine injections are affected. Those with allergies or anaphylaxis risks are at highest risk.
Check for SYMJEPI (epinephrine injection, USP) 0.15 mg (0.15 mg/0.3 mL) in two pre-filled syringes per carton. The product was manufactured for Adamis Pharmaceuticals Corp. and distributed by USWM, LLC.
Look for the product name, strength, and packaging details to confirm if it matches the recalled items.
Reach out to Adamis Pharmaceuticals Corporation for specific instructions on what to do next.
The recall is for potential needle clogging that could prevent proper epinephrine delivery during emergencies.
The official notice does not specify a remedy, so contact Adamis for instructions.
Check for SYMJEPI (epinephrine injection, USP) 0.15 mg (0.15 mg/0.3 mL) in two pre-filled syringes per carton.
We’ve drafted a message you can send Adamis to request your refund or repair — edit it as you like.
Subject: Recall D-0764-2022 — Adamis Adamis Hello, I own a Adamis that is covered by recall D-0764-2022 from Adamis. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
