CLASS II Drug recall · Reported 12 Jul 2017 · FDA Enforcement Report

Succinylcholine Chloride, 100 mg per, 20 mg per mL syringe recalled

Fagron Compounding Services is recalling Succinylcholine Chloride, 100 mg per, 20 mg per mL syringe, distributed nationwide in the US. The recall was initiated on 19 Jun 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: C274-000000331, BUD 08/30/2017; C274-000001274, BUD 09/07/2017; C274-000001326, BUD 09/14/2017
Quantity recalled1,056 5mL 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-0946-2017
FDA event ID
77584
Recalling firm
Fagron Compounding Services, Wichita, KS
Classification
Class II
Status
Terminated
Recall initiated
19 Jun 2017
FDA classified
6 Jul 2017
Reported
12 Jul 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility

Timeline

19 Jun 2017Recall initiated by company
6 Jul 2017Classified by FDA+17 days
12 Jul 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: voluntary recall initiated by the commercial supplier

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 Chloride, 100 mg per 5mL, 20 mg per mL syringe. IV Use Only. JCB Laboratories, 8710 E 34th St., N. Wichita, KS 67226 UPC 7335968405

Where it was distributed

Nationwide in the USA

Nationwide

Questions about this recall

Why was it recalled?

Lack Of Assurance Of Sterility: voluntary recall initiated by the commercial supplier

Which lots are affected?

Lot #: C274-000000331, BUD 08/30/2017; C274-000001274, BUD 09/07/2017; C274-000001326, BUD 09/14/2017

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 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.

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