FDA recall record

Ace Surgical Supply Co Succinylcholine 20 MG/ML INJ (QUELICIN), 10 ML Vials recall — FDA D-0071-2018

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

Class IIclassification
D-0071-2018official record ID
Nov 15, 2017report date

Recall record at a glance

Official recordD-0071-2018
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAce Surgical Supply Co., Inc.
Report dateNov 15, 2017
Recall initiation dateOct 24, 2017
Quantity200 vials (25 mislabeled vials)
LocationBrockton, MA, United States

Official product description

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

Why the product was recalled

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

Distribution information

Product was distributed throughout the United States.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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