Reported Mar 24, 2021 · Ongoing
Spironolactone Tablets, USP, 25 mg, packaged in
Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals · 1919 N Victory Pl · Burbank, CA · 91504-3425
Is this the product you have?
Spironolactone Tablets, USP, 25 mg, packaged in
3 of 3 products
| # | Product as published |
|---|---|
| 1 | 30-count bottles (NDC 63629-1064-01) |
| 2 | 60-count bottles (NDC 63629-1064-02) |
| 3 | 90-count bottles (NDC 63629-1064-03), Rx only, Manufactured by: Frontida BioPharm, Inc., Philadelphia, PA 19124 USA, Repackaged by: Bryant Ranch Prepack, Inc., Burbank, CA 91504 USA |
- Lot codes and dates
a) Lot #: 148969Exp 7/31/2022b) Lot #: 148791Exp 7/31/2022c) Lot #: 148991Exp 7/31/2022
- Amount recalled
- 35 bottles
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg may contain spironolactone 50 mg tablets.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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