Food recall: MYPROTEIN, MYPRE V2(TM) Net Wt. 17.6 Oz (1.1 lb) /500g, Blue Raspberry, preworkout, 500g, THE HUT GROUP(R), 1350 Cedar…
Class II FDA enforcement event 76825. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
A raw material initially failed testing Staphylococcus aureus. A retest was conducted with passing results but an out of specification investigation was not properly conducted leaving concern that the finished product could contain the bacterium.
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Armada Nutrition started this food recall on 23 Mar 2017. The firm address in the FDA record is in Spring Hill, TN. FDA put the recall in Class II. FDA event 76825 has 7 product records. The first FDA enforcement report date is 3 May 2017. The record gives the status Terminated, with the termination date 14 Feb 2018.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
CO, NJ, England, South Africa,
Recalling firm
Armada Nutrition, Spring Hill, TN.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
7 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-2146-2017 | MYPROTEIN, MYPRE V2(TM) Net Wt. 17.6 Oz (1.1 lb) /500g, Blue Raspberry, preworkout, 500g, THE HUT GROUP(R), 1350 Cedar Grove Park, Shepherdsville, KY, UPC 5 065104 570111 | 2,514 units | Class II | Terminated | 3 May 2017 |
| F-2147-2017 | BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe | 39,600 kg | Class II | Terminated | 3 May 2017 |
| F-2148-2017 | PERFORMIX(TM) CREA-BEAD, MULTI-PHASE CREATINE, UNFLAVOURED, (a) 30 SERVINGS, UPC 8 11274 02239 8; (b) 45 SERVINGS, Distributed by Performix LLC, 221 S. Cherokee St., Denver, CO 80223, UPC 8 11274 02203 8 | 39,273 units | Class II | Terminated | 3 May 2017 |
| F-2149-2017 | USN B4 -BOMB EXTREME PRE-WORKOUT, LIME LEMONADE FLAVOUR, 300g, USN North America, 1560 Sawgrass Corporation Pkwy, 4th Floor, Sunrise, FL, 33323 | 3,997 units | Class II | Terminated | 3 May 2017 |
| F-2150-2017 | Muscle Meds(TM) PERFORMANCE TECHNOLOGIES, BIOENGINEERED BEEF PROTEIN ISOLATE CARNIVOR(TM) Dietary Supplement, Net Wt. 2 lbs. (904.4g), ADVANCED FLAVOR TECHNOOGY FRUIT PUNCH, (a) 904.4g, (b)1808.8g, Manufactured for and Distributed by: MuscleMeds Performace Technologies 165 Clayton Road, West Caldwell, NJ 07006, UPC… | 1884 units | Class II | Terminated | 3 May 2017 |
| F-2151-2017 | MP MUSCLEPHARM, ASSAULT, ENERGY + STRENGTH, THE ATHLETES PRE-WORKOUT, GREEN APPLE, 11.75 OZ (O.73 LBS) (333G), Exclusively Developed & Manufactured for: MusclePharm Corp., 721 Ironton St., Denver, CO 80239, UPC 6 53341 04601 | 14,496 units | Class II | Terminated | 3 May 2017 |
| F-2152-2017 | PERFORMIX(TM) CREA-BEAD, MULTI-PHASE CREATINE, BLUE RAZZ ICE, NET WT 11.1 OZ (315G), Distributed by Performix LLC, 221 S. Cherokee St., Denver, CO 80223, UPC 8 11274 02204 5 | 19,552 units | Class II | Terminated | 3 May 2017 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Food events that started in 2017
- 599
- Share of these events in Class II
- 52%
- Product records in this event
- 7
- Events of the firm on the register
- 1
Official channels
- FDA enforcement report F-2146-2017The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
Follow by RSS:Food, drug and device recallsFDA Class I recalls
Cite this page
Recall Register. FDA enforcement event 76825. https://recallregister.com/fda/ii/76825/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
CO, NJ, England, South Africa,
- What quantity of product is in FDA event 76825?
- The event has 7 product records. The first record gives this quantity:
2,514 units
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2017 have the same class?
- 52% of the 599 food events that started in 2017 are in Class II.