FDAClass IIJanuary 17, 2018

Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride recall: Labeling Error

Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride 10 mL in Single Dose Syringe, Total Volume 10 mL, Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct.…

Why was Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride recalled?

Labeling: Incorrect or Missing Lot and/or Exp Date - product label was missing lot number and beyond use date.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot#: 20171013@30, Exp 12/27/2017

Product
Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride 10 mL in Single Dose Syringe, Total Volume 10 mL, Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct.…
Recalling firm
SCA Pharmaceuticals
Quantity
1248 syringes
Distribution
U.S.A. Nationwide
Recall date
January 17, 2018
Classification
Class II
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls