CLASS II Drug recall · Reported 13 Nov 2019 · FDA Enforcement Report

S-MICB12C/Cartinine 25/50/50/1/50MG/ML MDV INJ recalled

First Royal Care Co. LLC is recalling S-MICB12C/Cartinine 25/50/50/1/50MG/ML MDV INJ, distributed nationwide in the US. The recall was initiated on 12 Aug 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: S07092019DT@19, Exp 08/09/2019, S07292019DH@09, Exp 08/29/2019,
Quantity recalled2x30ml glass 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-0278-2020
FDA event ID
83669
Recalling firm
First Royal Care Co. LLC, Mesa, AZ
Classification
Class II
Status
Terminated
Recall initiated
12 Aug 2019
FDA classified
5 Nov 2019
Reported
13 Nov 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility

Timeline

12 Aug 2019Recall initiated by company
5 Nov 2019Classified by FDA+85 days
13 Nov 2019Published in enforcement report+8 days

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

Reason for recall

Lack of Assurance of Sterility

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

S-MICB12C/Cartinine 25/50/50/1/50MG/ML MDV INJ, Rx Only, 30ml, Red Mountain Compounding Rx.

Where it was distributed

Nationwide in the USA

Nationwide

Questions about this recall

Is S-MICB12C/Cartinine 25/50/50/1/50MG/ML MDV INJ recalled?

Yes. First Royal Care Co. LLC recalled S-MICB12C/Cartinine 25/50/50/1/50MG/ML MDV INJ on 12 Aug 2019. The recall is Class II and its status is Terminated. Recall number D-0278-2020.

Why was it recalled?

Lack of Assurance of Sterility

Which lots are affected?

Lot #: S07092019DT@19, Exp 08/09/2019, S07292019DH@09, Exp 08/29/2019,

Where was it sold?

Nationwide in the USA

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.

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