Dr Reddy's Laboratories Limited 2023-07-26 Health serious FDA
Health · FDA · Recall #FDA-D-0923-2023
Tizanidine Tablets USP, 4 mg, 1000-Count bottle, Rx Only, Manufactured by Dr. Reddy's… Recall
Issued July 26, 2023 · Dr Reddy's Laboratories Limited
In July 2023, Dr Reddy's Laboratories Limited recalled the Tizanidine Tablets USP, 4 mg, 1000-Count bottle, Rx Only, Manufactured by Dr. Reddy's…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Failed dissolution specification: Out of specification results observed in 24-month long term stability testing.
What you should do
- 1 Stop using Tizanidine Tablets USP, 4 mg, 1000-Count bottle, Rx Only, Manufactured by Dr. Reddy's… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Dr Reddy's Laboratories Limited to arrange your n/a. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (N/A):
Recall details
- Brand
- Dr Reddy's Laboratories Limited
- Category
- Health
- Recall date
- July 26, 2023
- Units affected
- Not reported
- Sold at
- Nationwide in the USA
- Recall number
- FDA-D-0923-2023
- Made in
- India
- Issuing agency
- FDA
In context
- Dr Reddy's Laboratories Limited has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.