FDAClass IIDecember 29, 2021

Rompe Pecho Max Multi-Symptoms Maximum Strength recall: Sterility Concern

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

Why was Rompe Pecho Max Multi-Symptoms Maximum Strength recalled?

Microbial Contamination of Non-Sterile Products

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot #: 19G219 Exp. July 2022

Product
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
Recalling firm
Efficient Laboratories, Inc.
Quantity
4,026 bottles
Distribution
Nationwide within the United States
Recall date
December 29, 2021
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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