Check the Batch
Class IIITerminated in FDA datasetDec 21, 2012

MET-Rx EXTREME THERMO RAGE WATERMELON DIETARY SUPPLEMENT, 8 FL. OZ. (240 mL) , Product Number 50390 (Bulk number 50389)

Recalling firm: NBTY Inc.

Why it was recalled

Acetobacter lovaniensis was detected in a sample of the product tested by a private laboratory. This is an issue of commercial spoilage.

Check the codes ↓

The exact product

MET-Rx EXTREME THERMO RAGE WATERMELON DIETARY SUPPLEMENT, 8 FL. OZ. (240 mL) , Product Number 50390 (Bulk number 50389), UPC 7 86560 50389 1, Label Revision 00B --- Manufactured in the USA by MET-RX Nutrition, Inc. Boca Raton, FL 33487

dietary supplementsfruitmelons

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

Lot # 430855, Expiration Date 12/21/12; Lot # 430856, Expiration Date 12/29/12

TypeCode / valueContext
UPC786560503891 SUPPLEMENT, 8 FL. OZ. (240 mL) , Product Number 50390 (Bulk number 50389), UPC 7 86560 50389 1, Label Revision 00B --- Manufactured in the USA by MET-RX Nutrition, Inc. Boca Raton, FL 33487
expiration12/21/12Lot # 430855, Expiration Date 12/21/12; Lot # 430856, Expiration Date 12/29/12
expiration12/29/12Lot # 430855, Expiration Date 12/21/12; Lot # 430856, Expiration Date 12/29/12
lot430855Lot # 430855, Expiration Date 12/21/12; Lot # 430856, Expiration Date 12/29/12
lot430856Lot # 430855, Expiration Date 12/21/12; Lot # 430856, Expiration Date 12/29/12

Recall details

Recall number
F-0980-2013
Event ID
64157
FDA status
Terminated
Initiated
Dec 21, 2012
Reported
Feb 13, 2013
Classified
Feb 5, 2013
Terminated
May 18, 2016
Quantity
40,668 bottles (shipped and sold in cases of 12)
Location
Bohemia, NY, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Nationwide and Puerto Rico

FDA source record · F-0980-2013

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.