F-1202-2015 Class III Terminated
FDA food recall F-1202-2015 was initiated by HVL, LLC on January 12, 2015 and is designated Class III. Reason for recall: Bottles contained a vegetarian digestive enzyme dietary supplement instead of melatonin. The recall status is terminated (terminated July 28, 2015). Affected quantity: 278.
Recall Details
- Product Type
- Food
- Report Date
- February 18, 2015
- Initiation Date
- January 12, 2015
- Termination Date
- July 28, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 278
Product Description
Melatonin Control- Released Tablets, 60 tablets, in plastic bottles, Manufactured by Douglas Laboratories, Pittsburgh, PA.
Reason for Recall
Bottles contained a vegetarian digestive enzyme dietary supplement instead of melatonin.
Distribution Pattern
Nationwide
Code Information
Lot # 50032151, exp. 12/20/2015