Rompe Pecho Expands Nationwide Recall Due to Microbial Contamination Concerns
Rompe Pecho CF, Rompe Pecho EX, Rompe Pecho MAX, and Rompe Pecho DM recalls have been expanded to cover 12 more lots distributed nationwide due to increased concerns regarding microbial contamination, according to manufacturer Efficient Laboratories.
Expansion of Efficient Laboratories Earlier Recalls
Efficient Laboratories is expanding its recall notice to consumers throughout the country. These lots were distributed in the year 2019. No adverse events have been reported to Efficient Laboratories to date.
Consumption of these specific lots may cause illness in rare circumstances. These products are meant to treat flu and common cold symptoms and come packaged in a box. The chart below details the twelve affected Rompe Pecho product lots:
- Rompe Pecho CF, Lots: 19F88 (Exp. Jun. 2022), 19G164 (Exp. Jul. 2022)
- Rompe Pecho DM, Lots: 19F168 (Exp. Jun. 2022), 19G145 (Exp. Jul. 2022), 19G361 (Exp. Jul. 2022), 19G449 (Exp. Jul. 2022), 19G491 (Exp. Jul. 2022)
- Rompe Pecho EX, Lots: 19H20 (Exp. Aug. 2022), 19J98 (Exp. Sep. 2022), 19A418 (Exp. Jan. 2022), 19E411 (Exp. May 2022)
- Rompe Pecho MAX, Lot: 19G219 (Exp. Jul. 2022)
On the bottom of the cartons, the lot number and expiration date are displayed. These Rompe Pecho products for recall were distributed to wholesalers and retailers nationwide.
What To Do with the Product Subject for Recall
Consumers who have Rompe Pecho EX, Rompe Pecho CF, Rompe Pecho DM, or Rompe Pecho MAX from these recalled lots should immediately discontinue the usage and discard the products.
The lots have been notified to Efficient Laboratories’ distributors. All distributors have reported that they do not have any product in inventory. Additionally, a review of certain businesses confirmed the absence of retail inventories.
Consumers with concerns or questions about Rompe Pecho Recall may contact Efficient Laboratories at (305) 805-3456 from 9 a.m. to 4:30 p.m. EST, Monday through Friday.
In addition, consumers should contact a physician or healthcare provider if they have any concerns about possible side effects from taking or using this medication.
Adverse events or product complaints related to this product may be submitted online to the MedWatch Adverse Event Reporting program of the FDA, via regular mail, or via fax.
This recall is being done with the knowledge of the FDA.
Editor’s Note on Rompe Pecho Recall:
This article informs you of the voluntary recall expansion conducted by Efficient Laboratories over microbial contamination concerning its products. We also suggest you read the Robitussin Maximum Strength Lawsuit.
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