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Moderate recall: A hazard has been identified, with no injuries reported yet. Follow the steps below.

The Ritedose Corporation 2022-04-13 Health moderate FDA
Health · FDA · Recall #FDA-D-0745-2022

23.4% Sodium Chloride Injection, 120 mEq per 30 mL (4 mEq/mL), 50 mL prefilled syring, Rx… Recall

Issued April 13, 2022 · The Ritedose Corporation

In April 2022, The Ritedose Corporation recalled the 23.4% Sodium Chloride Injection, 120 mEq per 30 mL (4 mEq/mL), 50 mL prefilled syring, Rx…, a moderate health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Labeling: Incorrect Barcode: Product barcode incorrectly identifies the product as rocuronium bromide injection 100 mg per 10 mL instead of sodium chloride injection 23.4%, 120 mEq per 30 mL.

What you should do

  1. 1 Stop using 23.4% Sodium Chloride Injection, 120 mEq per 30 mL (4 mEq/mL), 50 mL prefilled syring, Rx… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact The Ritedose Corporation to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
The Ritedose Corporation
Category
Health
Recall date
April 13, 2022
Units affected
Not reported
Sold at
Nationwide in the USA
Recall number
FDA-D-0745-2022
Made in
United States
Issuing agency
FDA

In context

  • The Ritedose Corporation has 2 recalls in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 870th Health recall we've logged in 2022.
Read the official FDA notice

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