LOW RISK
Terminated
F-1202-2015
Melatonin Control- Released Tablets, 60 tablets, in plastic bottles, Manufactured by Douglas Laboratories, Pittsburgh, PA.
Recalled by HVL, LLC
Classification
Class III — Products that are unlikely to cause any adverse health reaction, but that violate FDA labeling or manufacturing laws.
Reason for Recall
Bottles contained a vegetarian digestive enzyme dietary supplement instead of melatonin.
Product Details
Product Quantity
278
Product Type
Food
Code Info
Lot # 50032151, exp. 12/20/2015
Voluntary/Mandated
Voluntary: Firm initiated
Distribution & Geography
Distribution Pattern
Nationwide
Company Location
Pittsburgh, PA, 15205-9742
Timeline
Report Date
02/18/2015
Recall Initiated
01/12/2015
Classification Date
02/12/2015
Termination Date
07/28/2015
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: August 28, 2026
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