Food recall: AdvoCare Nighttime Recovery Amino Acid and Herbal Dietary Supplement Product code, P3201
FDA enforcement event 79734 is a food recall by AdvoCare International, LP of Plano, TX, initiated 30 Mar 2018 and classified Class II, with 2 product records.
FDA defines Class II as 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. 56% of the 578 food enforcement events initiated in 2018 carry the same class.
Status: Terminated, terminated 12 Sep 2018. Initiation: voluntary: firm initiated. AdvoCare International, LP has 2 enforcement events on this register, with a median of 2 product records per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
AdvoCare International, LP, Plano, TX.
Reason for recall
"Undeclared milk in a dietary supplement"
Distribution
"United States"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1124-2018 | AdvoCare Nighttime Recovery Amino Acid and Herbal Dietary Supplement Product code, P3201 | 48,176 units | Class II | Terminated | 2 May 2018 |
| F-1125-2018 | AdvoCare Muscle Strength Dietary Supplement with HMB and Suma Product code, P3221 | 15,640 units | Class II | Terminated | 2 May 2018 |
Context
Other enforcement events for AdvoCare International, LP
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 12 Nov 2018 | SleepWorks Liquid Vitamin & Mineral Herbal Supplement 12 single serving bottles - 2 Fl Oz (60 mL) Net 24 Fl Oz (720 mL), (81764) | Food | Class II | 1 |
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Undeclared milk in a dietary supplement"
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is 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.
Where was the product distributed?
FDA's distribution pattern field reads: "United States"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 12 Sep 2018. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.