FindMyRecallSubscribe
Class II: temporary or reversible health riskTerminated

Kabco Pharmaceuticals Perfect 3000 Vanilla Powder Recall

PERFECT 3000 VANILLA POWDER, FORMULA # 3101

Kabco Pharmaceuticals, Inc. · Amityville, NY

Risk level
Class II
Reported by FDA
Aug 7, 2013
Recall ID
F-1767-2013
Check your lot numberHow we source this data

Summary

Kabco Pharmaceuticals recalled Perfect 3000 Vanilla Powder starting Apr 9, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1767-2013 on Aug 7, 2013. Reason: Firm had distributed the bulk product in violation of the Consent Decree for Permanent Injunction (12-CV-3468). Status: Terminated.

Why it was recalled

Firm had distributed the bulk product in violation of the Consent Decree for Permanent Injunction (12-CV-3468).

Product description

PERFECT 3000 VANILLA POWDER, FORMULA # 3101. The product is loose powder packaged in bulk drum.

Lot numbers, UPCs & expiration codes

Lot BA13032004A and 13032004B

Where it was sold

New York

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-1767-2013
Classification
Class II
Status
Terminated
Recall initiated
Apr 9, 2013
FDA report date
Aug 7, 2013
Quantity
1813.60 Kilograms
Recall type
FDA Mandated
Recalling firm
Kabco Pharmaceuticals, Inc.

Original FDA data

Every field from FDA enforcement report F-1767-2013, exactly as published.

Show all FDA fields
City
Amityville
State
NY
Status
Terminated
Country
United States
Event ID
65763
Address
2000 New Horizons Blvd
Code information
Lot BA13032004A and 13032004B
Postal code
11701-1137
Report date
Aug 7, 2013
Product type
Food
Recall number
F-1767-2013
Classification
Class II
Recalling firm
Kabco Pharmaceuticals, Inc.
Product quantity
1813.60 Kilograms
Termination date
Mar 9, 2016
Reason for recall
Firm had distributed the bulk product in violation of the Consent Decree for Permanent Injunction (12-CV-3468).
Voluntary / mandated
FDA Mandated
Product description
PERFECT 3000 VANILLA POWDER, FORMULA # 3101. The product is loose powder packaged in bulk drum.
Distribution pattern
New York
Recall initiation date
Apr 9, 2013
Initial firm notification
Telephone
Center classification date
Jul 30, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1767-2013, published Aug 7, 2013. View the source record (openFDA) · FDA enforcement reports

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

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions.

How we source and update recall data · Report incorrect information

Other recent food recalls