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Class III: unlikely to cause harmTerminated

Hvl Melatonin Control- Released Tablets Recall

Melatonin Control- Released Tablets, 60 tablets, in plastic bottles, Manufactured by Do…

HVL, LLC · Pittsburgh, PA

Risk level
Class III
Reported by FDA
Feb 18, 2015
Recall ID
F-1202-2015
Check your lot numberHow we source this data

Summary

Hvl recalled Melatonin Control- Released Tablets starting Jan 12, 2015. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report F-1202-2015 on Feb 18, 2015. Reason: Bottles contained a vegetarian digestive enzyme dietary supplement instead of melatonin. Status: Terminated.

Why it was recalled

Bottles contained a vegetarian digestive enzyme dietary supplement instead of melatonin.

Product description

Melatonin Control- Released Tablets, 60 tablets, in plastic bottles, Manufactured by Douglas Laboratories, Pittsburgh, PA.

Lot numbers, UPCs & expiration codes

Lot # 50032151, exp. 12/20/2015

Where it was sold

Nationwide

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1202-2015
Classification
Class III
Status
Terminated
Recall initiated
Jan 12, 2015
FDA report date
Feb 18, 2015
Quantity
278
Recall type
Voluntary: Firm initiated
Recalling firm
HVL, LLC

Original FDA data

Every field from FDA enforcement report F-1202-2015, exactly as published.

Show all FDA fields
City
Pittsburgh
State
PA
Status
Terminated
Country
United States
Event ID
70272
Address
600 Boyce Rd
Code information
Lot # 50032151, exp. 12/20/2015
Postal code
15205-9742
Report date
Feb 18, 2015
Product type
Food
Recall number
F-1202-2015
Classification
Class III
Recalling firm
HVL, LLC
Product quantity
278
Termination date
Jul 28, 2015
Reason for recall
Bottles contained a vegetarian digestive enzyme dietary supplement instead of melatonin.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Melatonin Control- Released Tablets, 60 tablets, in plastic bottles, Manufactured by Douglas Laboratories, Pittsburgh, PA.
Distribution pattern
Nationwide
Recall initiation date
Jan 12, 2015
Initial firm notification
Telephone
Center classification date
Feb 12, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1202-2015, published Feb 18, 2015. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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