D-1087-2017 Class I Terminated
FDA drug recall D-1087-2017 was initiated by DYNAMIC TECHNICAL FORMULATIONS on May 19, 2017 and is designated Class I. Reason for recall: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplement: Product was tested by FDA and found to contain andarine and ostarine. The recall status is terminated (terminated May 7, 2020). Affected quantity: 728 bottles.
Recall details
- Product Type
- Drugs
- Report Date
- Aug 23, 2017
- Initiation Date
- May 19, 2017
- Termination Date
- May 7, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 728 bottles
Product description
Biotech Underground Tri-Ton Hardcore Formula capsules, 90-count bottle, Distributed by: Dynamic Technical Formulations 12850 Hwy 9 Suite 600-441 Alpharetta, GA 30004
Reason for recall
Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplement: Product was tested by FDA and found to contain andarine and ostarine.
Distribution pattern
U.S.A. nationwide
Code information
All lots
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-1087-2017
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026