GE Healthcare recalls Omnipaque 300 mg/mL injection due to particulate matter. Patients should not use affected lots; contact for replacement.
Presence of particulate matter
GE Healthcare is recalling Omnipaque 300 mg/mL injection products that contain particulate matter. This can cause serious health risks if injected into the body. Affected patients should stop using the product and contact their healthcare provider for a replacement.
Particulate matter in the injection can cause blockages or damage to blood vessels when injected. This poses a serious health risk, potentially leading to severe complications or injury.
Patients who have been prescribed Omnipaque 300 mg/mL injection by a healthcare provider. Those with the specific lot numbers listed in the recall are most at risk.
Check the product label for the lot numbers listed: 17225029 (exp. Sep 3, 2028), 17265376 (exp. Oct 3, 2028), and other specific lot numbers with their expiration dates.
Immediately stop using the recalled Omnipaque injection if you have the listed lot numbers.
Contact your healthcare provider for a replacement product or alternative treatment.
Particulate matter in the injection can cause blockages or damage to blood vessels when injected, posing a serious health risk.
Affected lot numbers include 17225029 (exp. Sep 3, 2028), 17265376 (exp. Oct 3, 2028), and other specific lot numbers listed in the recall.
Check the product label for the lot numbers listed in the recall: 17225029 (exp. Sep 3, 2028), 17265376 (exp. Oct 3, 2028), and other specific lot numbers with their expiration dates.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0447-2026 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall D-0447-2026 from GE 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.
