FDA Recall United States Terminated Historical recordClass II
Armada Nutrition
- Product
- PERFORMIX(TM) CREA-BEAD, MULTI-PHASE CREATINE, BLUE RAZZ ICE…
- Published
- May 3, 2017
- Distribution
- CO, NJ, England, South Africa,
Armada Nutrition Recall: 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.
United States
TerminatedClass II
- Company
- Armada Nutrition
- Product
- MP MUSCLEPHARM, ASSAULT, ENERGY + STRENGTH, THE ATHLETES PRE…
- Recall date
- March 23, 2017
- Terminated
- February 14, 2018
- Source
- FDA
Reason for recall
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.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | Not published in this source record | 14,496 units | lot IM448446, Exp 07/2018 |
Distribution
- CO
- NJ
- England
- South Africa
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-2151-2017
- Event ID
- 76825
- Status
- Terminated
- Classification
- Class II
- Company
- Armada Nutrition
- Product description
- 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
- Quantity
- 14,496 units
- Reason
- 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.
- Recall initiation date
- March 23, 2017
- Report date
- May 3, 2017
- Classification date
- Not published in this source record
- Termination date
- February 14, 2018
- Distribution pattern
- CO, NJ, England, South Africa,
- UPC, lot, and code information
- lot IM448446, Exp 07/2018
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 76825 with 6 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass II
Armada Nutrition
- Product
- Muscle Meds(TM) PERFORMANCE TECHNOLOGIES, BIOENGINEERED BEEF…
- Published
- May 3, 2017
- Distribution
- CO, NJ, England, South Africa,
FDA Recall United States Terminated Historical recordClass II
Armada Nutrition
- Product
- USN B4 -BOMB EXTREME PRE-WORKOUT, LIME LEMONADE FLAVOUR, 300…
- Published
- May 3, 2017
- Distribution
- CO, NJ, England, South Africa,
FDA Recall United States Terminated Historical recordClass II
Armada Nutrition
- Product
- PERFORMIX(TM) CREA-BEAD, MULTI-PHASE CREATINE, UNFLAVOURED,…
- Published
- May 3, 2017
- Distribution
- CO, NJ, England, South Africa,
FDA Recall United States Terminated Historical recordClass II
Armada Nutrition
- Product
- BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used…
- Published
- May 3, 2017
- Distribution
- CO, NJ, England, South Africa,
FDA Recall United States Terminated Historical recordClass II
Armada Nutrition
- Product
- MYPROTEIN, MYPRE V2(TM) Net Wt. 17.6 Oz (1.1 lb) /500g, Blu…
- Published
- May 3, 2017
- Distribution
- CO, NJ, England, South Africa,
Responsible company: Armada Nutrition
Other recalls from Armada Nutrition
FDA Recall United States Terminated Historical recordClass II
Armada Nutrition
- Product
- PERFORMIX(TM) CREA-BEAD, MULTI-PHASE CREATINE, BLUE RAZZ ICE…
- Published
- May 3, 2017
- Distribution
- CO, NJ, England, South Africa,
FDA Recall United States Terminated Historical recordClass II
Armada Nutrition
- Product
- Muscle Meds(TM) PERFORMANCE TECHNOLOGIES, BIOENGINEERED BEEF…
- Published
- May 3, 2017
- Distribution
- CO, NJ, England, South Africa,
FDA Recall United States Terminated Historical recordClass II
Armada Nutrition
- Product
- USN B4 -BOMB EXTREME PRE-WORKOUT, LIME LEMONADE FLAVOUR, 300…
- Published
- May 3, 2017
- Distribution
- CO, NJ, England, South Africa,
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Colorado | 1 |
| New Jersey | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
