Class II U.S. Food and Drug Administration

GE Healthcare Ireland Limited GE Healthcare Omnipaque Injection, 350 mg/mL recall: Presence of particulate matter

Recall published 6 months ago

Presence of particulate matter

The hazard: Sterility or particulate concern

The concern here is contamination of a product that bypasses the body’s normal defences, which is why the threshold for recalling it is low.

What the notice says: Presence of particulate matter

Why it matters: The product was made or packaged in conditions that cannot assure sterility, or visible particles were found in it. For anything injected, infused or used in the eye, that is a direct route for contamination into the body.

Symptoms and when to call a doctor

Watch for fever, chills, pain, redness, swelling or discharge at an injection site, and for a red, painful or suddenly blurred eye after using an eye product. Any of these needs same-day medical attention. Do not wait to see whether it settles, and tell the clinician which product and lot you used so it can be reported against the recall.

This page is general information, not medical advice. If you feel unwell, a clinician who can see you is the only person able to judge your case.

Recall details

Recall number
D-0448-2026
Published
April 15, 2026
Risk level
Class II
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
GE Healthcare Ireland Limited
Product type
Prescription & OTC drugs
Units affected
306,810 vials
Distribution
Nationwide
Made in
Ireland
Lot / code info
Lot# 17333197; Exp. December 10, 2028 Lot# 17333198; Exp. November 17, 2028 Lot# 17396945; Exp. December 18, 2028 Lot# 17396948; Exp. December 22, 2028 Lot# 17396953; Exp. January 11, 2029 Lot# 17396956; Exp. January 9, 2029 Lot# 17423503; Exp. January 1, 2029 Lot# 17423525; Exp. January 3, 2029 Lot# 17426429; Exp. January 1, 2029 Lot# 17426440; Exp. January 4, 2029 Lot# 17431310; Exp. January 11, 2029

Products covered by this recall

GE Healthcare Omnipaque (iohexol) Injection, 350 mg/mL (64.7%), Rx Only, Distributed by: GE Healthcare Inc., Marlborough, MA 01752 USA, NDC 0407-1414-91.

Check your product

The notice names 33 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

Lot or batch code

Usually ink-stamped near the seam, the cap or the bottom of the pack.

  • 17333197
  • 17333198
  • 17396945
  • 17396948
  • 17396953
  • 17396956
  • 17423503
  • 17423525
  • 17426429
  • 17426440
  • 17431310

Best-by / use-by date

Printed beside the lot code, not on the price sticker.

  • December 10
  • 2028 Lot# 17333198
  • November 17
  • 2028 Lot# 17396945
  • December 18
  • 2028 Lot# 17396948
  • December 22
  • 2028 Lot# 17396953
  • January 11
  • 2029 Lot# 17396956
  • January 9
  • 2029 Lot# 17423503
  • January 1
  • 2029 Lot# 17423525
  • January 3
  • 2029 Lot# 17426429
  • 2029 Lot# 17426440
  • January 4
  • 2029 Lot# 17431310
  • 2029 — 306

NDC number

On the carton and again on the bottle or blister label.

  • 0407-1414-91

Package size

Match the net weight or the piece count on the front of the pack.

  • 350 mg

Codes are lifted verbatim from the FDA — Drug enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Sterility

GE Healthcare Ireland Limited — The concern here is contamination of a product that bypasses the body’s normal defences, which is why the threshold for recalling it is low.

  1. Stop using the affected lot and check the lot number on your own carton or vial against the codes listed above.
  2. Call your prescriber or pharmacy today about a replacement from an unaffected lot — do not simply skip doses of a medicine you depend on.
  3. If you are a clinic or pharmacy, quarantine the stock and work it through your usual recall log.
  4. Report any infection or reaction you think the product caused to FDA MedWatch.

Getting a replacement supply

Do not let a refund question interrupt your treatment. Deal with the supply first and the money second.

  • Call the pharmacy before you run low. They can see which lot they dispensed to you and will usually swap it the same day.
  • Insurers do not normally count a recall replacement against a refill limit. If one is refused, ask the pharmacist to call it through as a recall override.
  • Over-the-counter products are refunded at the till like any other purchase; the recall notice on your phone is enough to explain the return.
  • If the manufacturer runs a direct reimbursement form, it will be linked from the official notice on this page.

Company contact: GE Healthcare Ireland Limited — Ida Business Park, Carrigtwohill

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Drug enforcement record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was GE Healthcare Ireland Limited prescription & otc drugs recalled?

Presence of particulate matter Presence of particulate matter

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: lot code 17333197, 17333198, 17396945; best-by date December 10 or 2028 Lot# 17333198. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Stop using the affected lot and check the lot number on your own carton or vial against the codes listed above.

Can I get my money back?

Call the pharmacy before you run low. They can see which lot they dispensed to you and will usually swap it the same day.

Where was the recalled product sold?

It was distributed nationwide.

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