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Class II: temporary or reversible health riskTerminated

Efficient Laboratories Rompe Pecho Max Multi-Symptoms Maximum Recall

Rompe Pecho Max Multi-Symptoms Maximum Strength, 8 Fl

Efficient Laboratories, Inc. · Miami, FL

Risk level
Class II
Reported by FDA
Dec 29, 2021
Recall ID
D-0293-2022
Check your lot numberHow we source this data

Summary

Efficient Laboratories recalled Rompe Pecho Max Multi-Symptoms Maximum starting Aug 24, 2021. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0293-2022 on Dec 29, 2021. Reason: Microbial Contamination of Non-Sterile Products. Status: Terminated.

Why it was recalled

Microbial Contamination of Non-Sterile Products

Product description

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

Lot numbers, UPCs & expiration codes

Lot #: 19G219 Exp. July 2022

Where it was sold

Nationwide within the United States

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0293-2022
Classification
Class II
Status
Terminated
Recall initiated
Aug 24, 2021
FDA report date
Dec 29, 2021
Quantity
4,026 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Efficient Laboratories, Inc.

Original FDA data

Every field from FDA enforcement report D-0293-2022, exactly as published.

Show all FDA fields
City
Miami
State
FL
Status
Terminated
Country
United States
Event ID
89205
Address
7715 NW 64th St
Code information
Lot #: 19G219 Exp. July 2022
Postal code
33166-2719
Report date
Dec 29, 2021
Product type
Drugs
Recall number
D-0293-2022
Classification
Class II
Recalling firm
Efficient Laboratories, Inc.
Product quantity
4,026 bottles
Termination date
Dec 8, 2022
Reason for recall
Microbial Contamination of Non-Sterile Products
Voluntary / mandated
Voluntary: Firm initiated
Product description
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
Distribution pattern
Nationwide within the United States
Recall initiation date
Aug 24, 2021
Initial firm notification
Letter
Center classification date
Dec 22, 2021

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0293-2022, published Dec 29, 2021. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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