Accord Healthcare recalls Atropine Sulfate Injection vials due to fiber particles. This may cause serious injury if injected. Stop using immediately and contact the manufacturer.
Presence of Particulate Matter: Particulate matter identified as fiber.
Accord Healthcare is recalling Atropine Sulfate Injection vials that contain fiber particles. This risk could cause serious injury if the medication is injected. Affected vials have specific lot numbers and expiration dates.
Fiber particles in the injection vials could enter the bloodstream during medical procedures. This may cause serious injury or death if the particles are injected into the body.
Healthcare professionals who use these vials for medical injections. Patients receiving injections from these vials are at risk of serious injury.
Check for vials labeled 'Atropine Sulfate Injection, USP 8 mg per 20 mL (0.4 mg per mL), 20 mL Multiple Dose Vials, Rx only'. Look for lot numbers M2210154 (expiring 06/2025) or M2212575 (expiring 08/2025).
Discard the vials if you have them and contact Accord Healthcare for a replacement.
The vials contain fiber particles that could enter the bloodstream during injection, posing a serious injury risk.
Look for vials labeled 'Atropine Sulfate Injection, USP 8 mg per 20 mL (0.4 mg per mL), 20 mL Multiple Dose Vials, Rx only' with lot numbers M2210154 (expiring 06/2025) or M2212575 (expiring 08/2025).
The recall record does not specify a return process, but you should discard the vials immediately and contact Accord Healthcare for a replacement.
We’ve drafted a message you can send Accord Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0917-2023 — Accord Healthcare Accord Healthcare Hello, I own a Accord Healthcare that is covered by recall D-0917-2023 from Accord Healthcare. 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.
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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.
