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Serious recall: Injury is possible or has been reported. Take action promptly.

Aurobindo Pharma USA Inc. 2024-05-15 Health serious FDA
Health · FDA · Recall #FDA-D-0492-2024

Clorazepate Dipotassium Tablets, USP, 7.5 mg, a) 100 tablets per bottle, NDC… Recall

Issued May 15, 2024 · Aurobindo Pharma USA Inc.

In May 2024, Aurobindo Pharma USA Inc. recalled the Clorazepate Dipotassium Tablets, USP, 7.5 mg, a) 100 tablets per bottle, NDC…, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Discoloration: Dotted and yellow spots on tablets

What you should do

  1. 1 Stop using Clorazepate Dipotassium Tablets, USP, 7.5 mg, a) 100 tablets per bottle, NDC… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Aurobindo Pharma USA Inc. 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
Aurobindo Pharma USA Inc.
Category
Health
Recall date
May 15, 2024
Units affected
Not reported
Sold at
Nationwide in the USA
Recall number
FDA-D-0492-2024
Made in
United States
Issuing agency
FDA

In context

  • Aurobindo Pharma USA Inc. has 2 recalls in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 737th Health recall we've logged in 2024.
Read the official FDA notice

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