Bracco Diagnostics recalls

Bracco Diagnostics has 7 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 4 Apr 2018. The most frequent reason is potency & assay.

Total recalls7since 2012

Last 12 months0reported

Class I00% of total

Ongoing0latest 4 Apr 2018

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 4 57%Class III 3 43%

Why bracco diagnostics is recalled

Product types

Injectable & IV Drugs229%
Creams, Ointments & Gels114%

Brands

By year

2018114%
2014114%
2013229%
2012343%

All bracco diagnostics recalls, newest first

7 total

Reported	Class	Recall	Company	Reason	Where
4 Apr 2018Drug	CLASS II	E-Z-Paste Barium Sulfate Esophageal Cream (60% w/w) tube recalledE-z-paste	Bracco Diagnostics	Potency & Assay	Nationwide
19 Feb 2014Drug	CLASS III	VoLumen Barium Sulfate Suspension 1 % w/v, 1 ww/w) recalled	Bracco Diagnostics	Potency & Assay	Nationwide
28 Aug 2013Drug	CLASS III	Tagitol V Barium Sulfate Suspension (40% w/v recalled	Bracco Diagnostics	Potency & Assay	Nationwide
21 Aug 2013Drug	CLASS II	Gastrografin (Diatrizoate Meglumine recalled by Bracco DiagnosticsGastrografin	Bracco Diagnostics	Particulate Matter	Nationwide
3 Oct 2012Drug	CLASS II	Cardiogen-82 (Rubidium Rb 82 Generator), 140 millicurie recalledCardiogen-82	Bracco Diagnostics	Sterility	Nationwide
5 Sep 2012Drug	CLASS II	Multihance Multipack (gadobenate dimeglumine) injection recalledMultihance	Bracco Diagnostics	Sterility	Nationwide
5 Sep 2012Drug	CLASS III	multihance (gadobenate dimeglumine) injection, 529 mg/mL recalledMultihance	Bracco Diagnostics	Packaging Defects	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.