Spectrum recalls epinephrine (L-Adrenaline) due to discoloration that could make it less effective. Affected lots expire by Sep 2023 or Mar 2023. Check your amber glass bottles with vacuum pouches.
Discoloration: Product complaints of the repackaged Epinephrine API being discolored which could result in less effective product
Spectrum is recalling epinephrine injections that may have turned discolored, making them less effective. This could be risky for people who need the medication during emergencies.
The epinephrine may have changed color after repackaging, which could reduce its effectiveness. This means it might not work properly when needed in an emergency.
People with prescriptions for epinephrine injections, especially those using the product for emergencies like anaphylaxis. Those with the specific lot numbers listed are most at risk.
Check for amber glass bottles with vacuum-sealed pouches labeled as 100 G, 1 G, 25 G, or 5 G. Look for lot numbers 2KL0353 (expires Sep 2023) or 2KF0151 (expires Mar 2023).
Look for lot numbers 2KL0353 (expires Sep 2023) or 2KF0151 (expires Mar 2023) on the packaging.
The recall states discoloration could make the product less effective, but it doesn't say it's unsafe. The product is still intended for emergency use.
Check for amber glass bottles with vacuum-sealed pouches labeled 100 G, 1 G, 25 G, or 5 G, and lot numbers 2KL0353 or 2KF0151.
The recall doesn't specify a discard or return action. You should check the lot number to see if it's affected.
We’ve drafted a message you can send Spectrum to request your refund or repair — edit it as you like.
Subject: Recall D-0180-2023 — Spectrum Spectrum Hello, I own a Spectrum that is covered by recall D-0180-2023 from Spectrum. 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.