CLASS II Drug recall · Reported 15 Nov 2017 · FDA Enforcement Report

Succinylcholine 20 MG/ML INJ (Quelicin) Vials recalled

Ace Surgical Supply is recalling Succinylcholine 20 MG/ML INJ (Quelicin) Vials, distributed nationwide in the US. The recall was initiated on 24 Oct 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # 64340EV, exp 07/2018 ACE ITEM # 1671018
Quantity recalled200 vials (25 mislabeled 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-0071-2018
FDA event ID
78376
Recalling firm
Ace Surgical Supply, Brockton, MA
Classification
Class II
Status
Terminated
Recall initiated
24 Oct 2017
FDA classified
7 Nov 2017
Reported
15 Nov 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

24 Oct 2017Recall initiated by company
7 Nov 2017Classified by FDA+14 days
15 Nov 2017Published 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

Labeling: Incorrect or Missing Lot and/or Exp Date; incorrect expiration date on the labeling of the outer poly bag

Product as listed by the FDA

Succinylcholine 20 MG/ML INJ (QUELICIN), 10 ML Vials, Rx only, Distributed by: ACE Surgical Co., Inc., Brockton, MA

Where it was distributed

Product was distributed throughout the United States.

Nationwide

Questions about this recall

Why was it recalled?

Labeling: Incorrect or Missing Lot and/or Exp Date; incorrect expiration date on the labeling of the outer poly bag

Which lots are affected?

Lot # 64340EV, exp 07/2018 ACE ITEM # 1671018

Where was it sold?

Product was distributed throughout 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.

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