Rompe Pecho Max Multi-Symptoms Maximum Strength recalled over sterility concerns
- Recall date
- August 24, 2021
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Efficient Laboratories, Inc. recalls Rompe Pecho Max Multi-Symptoms Maximum Strength, 8 Fl. Oz. (237 mL) bottles, Distributed by: Efficient Laboratories, In…
- Recall number
- D-0293-2022
- FDA classification
- Class II
- Brand / firm
- Efficient Laboratories, Inc.
- Sold / distributed
- Nationwide within the United States
Why it was recalled
Microbial Contamination of Non-Sterile Products
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Rompe Pecho Max Multi-Symptoms Maximum Strength, 8 Fl. Oz. (237 mL) bottles, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166 UPC 0 00856 00309 5, NDC 58593-828-08
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