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Class I: serious health riskOngoing

Glades Drugs Vitamin Supplement Recall

Vitamin Supplement (Vial) D3, (cholecalciferol (vit D3)/lipoic acid/ubiquinol/ methylco…

Glades Drugs Inc. · Pahokee, FL

Risk level
Class I
Reported by FDA
Feb 24, 2016
Recall ID
D-0669-2016
Check your lot numberHow we source this data

Summary

Glades Drugs recalled Vitamin Supplement starting Nov 6, 2015. The FDA classified it as Class I (serious health risk) and published enforcement report D-0669-2016 on Feb 24, 2016. Reason: Superpotent Drug: The vitamin supplement contains an extremely high level of vitamin D3 (Cholecalciferol). Status: Ongoing.

Why it was recalled

Superpotent Drug: The vitamin supplement contains an extremely high level of vitamin D3 (Cholecalciferol).

Product description

Vitamin Supplement (Vial) D3, (cholecalciferol (vit D3)/lipoic acid/ubiquinol/ methylcobalamin/pyridoxine/methionine/inositol/choline bitartrate USP) capsules, 60, 120 or 180 count vials, Glades Drugs, 109 S. Lake Ave., Pahokee, FL 33476.

Lot numbers, UPCs & expiration codes

AICACABF@3, AICECABF@2, AJBFCABF@4, ABCCABF@4, AICACABF@5, AICECABF@3, AJBHCABF@2, ABCCABF@5, AICBCABF@1, AICECABF@4, AJCBCABF@1, ABGCABF@4, AICBCABF@2, AICECABF@5, JCBCABF@2, BACDCABF@5, AICBCABF@3, AICICABF@3, BAAGCABF@2, BADACABF@3, AICBCABF@4, AJADCABF@1, BAAICABF@1, BACCABF@3, AICECABF@1, AJBECABF@6, BABCCABF@2 and BBAECABF@5, Exp 02/20/2016

Where it was sold

New York and Georgia

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0669-2016
Classification
Class I
Status
Ongoing
Recall initiated
Nov 6, 2015
FDA report date
Feb 24, 2016
Quantity
7800 capsules
Recall type
Voluntary: Firm initiated
Recalling firm
Glades Drugs Inc.

Original FDA data

Every field from FDA enforcement report D-0669-2016, exactly as published.

Show all FDA fields
City
Pahokee
State
FL
Status
Ongoing
Country
United States
Event ID
72737
Address
109 S Lake Ave
Code information
AICACABF@3, AICECABF@2, AJBFCABF@4, ABCCABF@4, AICACABF@5, AICECABF@3, AJBHCABF@2, ABCCABF@5, AICBCABF@1, AICECABF@4, AJCBCABF@1, ABGCABF@4, AICBCABF@2, AICECABF@5, JCBCABF@2, BACDCABF@5, AICBCABF@3, AICICABF@3, BAAGCABF@2, BADACABF@3, AICBCABF@4, AJADCABF@1, BAAICABF@1, BACCABF@3, AICECABF@1, AJBECABF@6, BABCCABF@2 and BBAECABF@5, Exp 02/20/2016
Postal code
33476-1803
Report date
Feb 24, 2016
Product type
Drugs
Recall number
D-0669-2016
Classification
Class I
Recalling firm
Glades Drugs Inc.
Product quantity
7800 capsules
Reason for recall
Superpotent Drug: The vitamin supplement contains an extremely high level of vitamin D3 (Cholecalciferol).
Voluntary / mandated
Voluntary: Firm initiated
Product description
Vitamin Supplement (Vial) D3, (cholecalciferol (vit D3)/lipoic acid/ubiquinol/ methylcobalamin/pyridoxine/methionine/inositol/choline bitartrate USP) capsules, 60, 120 or 180 count vials, Glades Drugs, 109 S. Lake Ave., Pahokee, FL 33476.
Distribution pattern
New York and Georgia
Recall initiation date
Nov 6, 2015
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Feb 16, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0669-2016, published Feb 24, 2016. View the source record (openFDA) · FDA enforcement reports

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

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