Rompe Pecho Cold Remedy Products [US]:

US FlagUS/Silver Spring: Rompe Pecho Cold Remedy Recall [US]Efficient Laboratories, a Miami, Florida establishment, recalls certain batch/lots of Rompe Pecho CF, Rompe Pecho EX, Rompe Pecho MAX and Rompe Pecho DM Cold Remedy drug products from the American marketplace due to suspected unspecified microbial contamination and consequential risks of Gram-positive or Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

FDA: http://ht.ly/buRb30s3NRf

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/efficient-laboratories-inc-expands-voluntary-nationwide-recall-consumers-include-twelve-additional

Additional information:
The US Food and Drug Administration (“FDA”) reports the following over-the-counter (“OTC”) Cold Remedy drugs are subject to this recall:

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