openFDA Food Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
food · product 1 of 7
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
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.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
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.
Code information
lot IM475137, Exp 01/2019
Distribution pattern
CO, NJ, England, South Africa,
food · product 2 of 7
BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe
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.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
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.
Code information
lot IM459653, Exp 08/2018 and lot IM470108, Exp 10/2018
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.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
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.
Code information
(a) lot IM458501, Exp 10/2018 (b) lot IM447128, Exp 07/2018, lot IM445515
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.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
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.
Code information
lot IM453078, Exp 08/2018
Distribution pattern
CO, NJ, England, South Africa,
food · product 5 of 7
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 08 91597 00214 6
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.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
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.
Code information
(a) lot IM445587, Exp 07/2019 (b) lot IM449808, Exp 07/2019
Distribution pattern
CO, NJ, England, South Africa,
food · product 6 of 7
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
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.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
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.
Code information
lot IM448446, Exp 07/2018
Distribution pattern
CO, NJ, England, South Africa,
food · product 7 of 7
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
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.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
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.
