CLASS II Drug recall · Reported 8 Nov 2017 · FDA Enforcement Report

SUCcinylcholine 20 mg per mL, Total Volume recalled

SCA Pharmaceuticals is recalling SUCcinylcholine 20 mg per mL, Total Volume in single-dose syringe, (SUCcinylcholine 200 mg, distributed nationwide in the US. The recall was initiated on 19 Oct 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: 20170726@35 BUD: 10/24/2017
Quantity recalled1248 syringes

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-0059-2018
FDA event ID
78320
Recalling firm
SCA Pharmaceuticals, Little Rock, AR
Classification
Class II
Status
Terminated
Recall initiated
19 Oct 2017
FDA classified
2 Nov 2017
Reported
8 Nov 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility

Timeline

19 Oct 2017Recall initiated by company
2 Nov 2017Classified by FDA+14 days
8 Nov 2017Published 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

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

SUCcinylcholine 20 mg per mL, Total Volume 10 mL in single-dose syringe, (SUCcinylcholine 200 mg / 10 ml) Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR NDC 70004-0910-29

Where it was distributed

Nationwide in the United States

Nationwide

Questions about this recall

Why was it recalled?

Lack Of Assurance Of Sterility.

Which lots are affected?

Lot: 20170726@35 BUD: 10/24/2017

Where was it sold?

Nationwide in the United States

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

Other products in this recall event

9 other products · FDA event 78320

This product is part of a recall event; the main page for the event is fentaNYL as citrate 2 mcg / mL, ROPIVacaine HCl recalled.

More recalls from SCA Pharmaceuticals

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