New! Rompe Pecho MAX Multi Symptoms recalled over sterility concerns
- Recall date
- January 31, 2020
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Efficient Laboratories, Inc. recalls New! Rompe Pecho MAX Multi Symptoms, 8 FL. Oz (237 mL) bottle, Distributed by: Efficient Laboratories, Inc. Miami, FL 3…
- Recall number
- D-0847-2020
- FDA classification
- Class II
- Brand / firm
- Efficient Laboratories, Inc.
- Sold / distributed
- Distributed Nationwide in the USA
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
New! Rompe Pecho MAX Multi Symptoms, 8 FL. Oz (237 mL) bottle, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166. UPC 0 00856 00309 5
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