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Serious recall: Injury is possible or has been reported. Take action promptly.

GE Healthcare Ireland Limited 2026-04-15 Health serious FDA
Health · FDA · Recall #FDA-D-0448-2026

GE Healthcare Omnipaque (iohexol) Injection, 350 mg/mL (64.7%), Rx Only, Distributed by:… Recall

Issued April 15, 2026 · GE Healthcare Ireland Limited

In April 2026, GE Healthcare Ireland Limited recalled the GE Healthcare Omnipaque (iohexol) Injection, 350 mg/mL (64.7%), Rx Only, Distributed by:…, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Presence of particulate matter

What you should do

  1. 1 Stop using GE Healthcare Omnipaque (iohexol) Injection, 350 mg/mL (64.7%), Rx Only, Distributed by:… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact GE Healthcare Ireland Limited to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
GE Healthcare Ireland Limited
Category
Health
Recall date
April 15, 2026
Units affected
Not reported
Sold at
U.S. Nationwide.
Recall number
FDA-D-0448-2026
Made in
Ireland
Issuing agency
FDA

In context

  • GE Healthcare Ireland Limited has 1 recall in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 356th Health recall we've logged in 2026.
Read the official FDA notice

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