Reported Apr 15, 2026 · Ongoing

GE Healthcare Omnipaque (iohexol) Injection, 300 mg/mL (64.7%), Rx Only, Distributed by: GE Healthcare Inc.,…

GE Healthcare Ireland Limited

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: GE Healthcare Ireland Limited · Ida Business Park · Carrigtwohill · N/A

Is this the product you have?

  • GE Healthcare Omnipaque (iohexol) Injection, 300 mg/mL (64.7%), Rx Only
  • Distributed byGE Healthcare Inc., Marlborough, MA 01752 USA, NDC 0407-1413-63
Lot codes and dates

19 of 19 products

Products covered by this recall
#Product as published
1Lot# 17225029
2Exp. September 3, 2028 Lot# 17265376
3Exp. October 3, 2028 Lot# 17270885
4Exp. September 10, 2028 Lot# 17292246
5Exp. October 4, 2028 Lot# 17301805
6Exp. October 18, 2028 Lot# 17301807
7Exp. September 7, 2028 Lot# 17301810
8Exp. October 20, 2028 Lot# 17304992
9Exp. October 5, 2028 Lot# 17304993
10Exp. October 19, 2028 Lot# 17304996
11Exp. November 25, 2028 Lot# 17321225
12Exp. September 8, 2028 Lot# 17333589
13Exp. November 24, 2028 Lot# 17333611
14Exp. November 26. 2028 Lot# 17333613
15Exp. November 23. 2028 Lot# 17357000
16Exp. December 5, 2028 Lot# 17366399
17Exp. December 14, 2028 Lot# 17376486
18Exp. December 14, 2028 Lot# 17404114
19Exp. December 6, 2028
Amount recalled
866,570 vials

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

Presence of particulate matter

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Data as of Sep 19, 6:36 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.