Ignite High Endurance Pre-Workout Supplement with Caffeine, brand Back to Health, Net wt. 1 lb.
Recalling firm: Independent Nutrition, Inc.
Ignite High Endurance Pre-Workout Supplement with Caffeine dietary supplement product is recalled because label declared WHEY protein but do not declare milk.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 11, 2018.
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801650015402, 801650015419FDA code information
Back to Health brand lot #: 1502014, 1503001, 1512022, 1605004, 1105007, and 1711009. Private label brands: firm did not provide lot codes.
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Full FDA record and distribution details
Original product description
Ignite High Endurance Pre-Workout Supplement with Caffeine, brand Back to Health, Net wt. 1 lb. UPC 8 01650 01540 2. Ignite High Endurance Pre-Workout Supplement with CAFFEINE, brand Muscle Sports & Nutrition (MSN), Net wt. 1 lb. UPC 8 01650 01540 2 and UPC 8 01650 01541 9.
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 801650015402 | Pre-Workout Supplement with Caffeine, brand Back to Health, Net wt. 1 lb. UPC 8 01650 01540 2. Ignite High Endurance Pre-Workout Supplement with CAFFEINE, brand Muscle Sports & Nutrition (MSN), Net wt. 1 lb. UP |
| UPC | 801650015402 | plement with CAFFEINE, brand Muscle Sports & Nutrition (MSN), Net wt. 1 lb. UPC 8 01650 01540 2 and UPC 8 01650 01541 9. |
| UPC | 801650015419 | rand Muscle Sports & Nutrition (MSN), Net wt. 1 lb. UPC 8 01650 01540 2 and UPC 8 01650 01541 9. |
Original FDA recall reason
Ignite High Endurance Pre-Workout Supplement with Caffeine dietary supplement product is recalled because label declared WHEY protein but do not declare milk.
Recall details
- Recall number
- F-1174-2018
- Event ID
- 79686
- FDA status
- Terminated
- Initiated
- Mar 28, 2018
- Reported
- May 9, 2018
- Classified
- May 3, 2018
- Terminated
- Sep 11, 2018
- Quantity
- Undetermined
- Location
- Eugene, OR, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Telephone
Where it was distributed
CA, FL, MO, NJ, OR, TX
Data updated September 16, 2026. View official FDA data ↗
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