CLASS II Drug recall · Reported 13 Sep 2017 · FDA Enforcement Report

Curcumin Emulsion 10mg/ml Injection recalled by ImprimisRx CA, Inc

ImprimisRx CA, Inc is recalling Curcumin Emulsion 10mg/ml Injection, Sterile Multiple Dose Vial, For Slow IV, distributed nationwide in the US. The recall was initiated on 23 Jun 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes03212017@21B Exp:6/19/2017; 03232017@19B Exp:6/21/2017; 03292017@27B Exp:6/27/2017; 03292017@9B Exp:6/27/2017; 04042017@21B Exp:7/3/2017; 04122017@22B Exp:7/11/2017; 04132017@14B Exp:7/12/2017; 04192017@37B Exp:7/18/2017; 04192017@17B Exp:7/18/2017; 04242017@18B Exp:7/23/2017

Quantity recalled2608 vials

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number: D-1130-2017
FDA event ID: 77647
Recalling firm: ImprimisRx CA, Inc, Irvine, CA
Classification: Class II
Status: Terminated
Recall initiated: 23 Jun 2017
FDA classified: 7 Sep 2017
Reported: 13 Sep 2017
Type: Voluntary: Firm initiated
Customers notified by: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category: Labeling Errors
Drug class: Injectable & IV Drugs

Timeline

23 Jun 2017	Recall initiated by company
7 Sep 2017	Classified by FDA	+76 days
13 Sep 2017	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier

Product as listed by the FDA

Curcumin Emulsion 10mg/ml Injection, Sterile 10 mL Multiple Dose Vial, For Slow IV Administration, Compounded for a licensed professional or patient use by ImprimisRx, Irvine, CA

Where it was distributed

Nationwide

Questions about this recall

Is Curcumin Emulsion 10mg/ml Injection, Sterile Multiple Dose Vial, For Slow IV recalled?

Yes. ImprimisRx CA, Inc recalled Curcumin Emulsion 10mg/ml Injection, Sterile Multiple Dose Vial, For Slow IV on 23 Jun 2017. The recall is Class II and its status is Terminated. Recall number D-1130-2017.

Why was it recalled?

Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier

Which lots are affected?

03212017@21B Exp:6/19/2017; 03232017@19B Exp:6/21/2017; 03292017@27B Exp:6/27/2017; 03292017@9B Exp:6/27/2017; 04042017@21B Exp:7/3/2017; 04122017@22B Exp:7/11/2017; 04132017@14B Exp:7/12/2017; 04192017@37B Exp:7/18/2017; 04192017@17B Exp:7/18/2017; 04242017@18B Exp:7/23/2017

Where was it sold?

Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from ImprimisRx CA, Inc

All 4

Reported	Class	Recall	Company	Reason	Where
13 Sep 2017Drug	CLASS II	Timolol-Brimonidine-Dorzolamide-Latanoprost recalled	ImprimisRx CA, Inc	Labeling Errors	Nationwide
13 Sep 2017Drug	CLASS II	Timolol-Latanoprost PF Solution 5-0.005)%, Ophthalmic Drops recalled	ImprimisRx CA, Inc	Labeling Errors	Nationwide
13 Sep 2017Drug	CLASS II	Latanoprost PF Solution, 005%, Ophthalmic Drops in Sterile recalled	ImprimisRx CA, Inc	Labeling Errors	Nationwide