Why it was recalled
PURE GHEE, INC. VOLUNTARY RECALLS VRINDAVAN COW GHEE DUE TO AN UNDECLARED MILK ALLERGEN
Product description
"VRINDAVAN" COW GHEE, Ingredients: 100% clarified butter
Lot numbers, UPCs & expiration codes
CODE: 2 fl. oz. (UPC #753642000999) 8 fl. oz. (UPC #753642001002) 16 fl. oz. (UPC #753642001002) 32 fl. oz. (UPC #753642001019) 64 fl. oz. (UPC #753642001033) 128 fl. oz. (UPC #753642001040)
Where it was sold
The product was distributed in NJ and NY
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-0086-2017
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Sep 8, 2016
- FDA report date
- Oct 19, 2016
- Quantity
- 347 Cases
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Pure Ghee, Inc.
Original FDA data
Every field from FDA enforcement report F-0086-2017, exactly as published.
Show all FDA fields
- City
- Wheeling
- State
- WV
- Status
- Terminated
- Country
- United States
- Event ID
- 75269
- Address
- 6018 Big Wheeling Creek Rd
- Code information
- CODE: 2 fl. oz. (UPC #753642000999) 8 fl. oz. (UPC #753642001002) 16 fl. oz. (UPC #753642001002) 32 fl. oz. (UPC #753642001019) 64 fl. oz. (UPC #753642001033) 128 fl. oz. (UPC #753642001040)
- Postal code
- 26003-7277
- Report date
- Oct 19, 2016
- Product type
- Food
- Recall number
- F-0086-2017
- Classification
- Class II
- Recalling firm
- Pure Ghee, Inc.
- Product quantity
- 347 Cases
- Termination date
- Feb 9, 2017
- Reason for recall
- PURE GHEE, INC. VOLUNTARY RECALLS VRINDAVAN COW GHEE DUE TO AN UNDECLARED MILK ALLERGEN
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- "VRINDAVAN" COW GHEE, Ingredients: 100% clarified butter
- Distribution pattern
- The product was distributed in NJ and NY
- Recall initiation date
- Sep 8, 2016
- Initial firm notification
- Center classification date
- Oct 12, 2016