Organic Cold brew BUDDY BREW COFFEE BOLT Original 10.5 oz. cans and 5 and 7.5 gallon kegs

Class I - Dangerous
Recalled: December 19, 2019 Buddy Brew Coffee Beverages

What Should You Do?

  1. Check if you have this product:
    Manufacturing Lot Number and Best Used By 104 12/24/19 105 12/25/19 106 12/26/19 107 12/29/19 110 1/2/20 111 1/3/20 112 1/6/20 114 1/9/20 115 1/10/20 116 1/13/20 117 1/14/20 118 1/15/20 119 1/16/20 120 1/17/20 121 1/20/20 123 1/20/20 124 1/23/20 125 1/24/20 126 1/27/20 127 1/28/20 128 1/29/20 129 1/30/20 130 1/31/20 131 2/3/20 132 2/4/20 133 2/5/20 134 2/6/20 135 2/7/20 136 2/10/20 137 2/12/20
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Buddy Brew Coffee
Reason for Recall:
Product has potential to be contaminated with bacteria.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Organic Cold brew BUDDY BREW COFFEE BOLT Original 10.5 oz. cans and 5 and 7.5 gallon kegs

Product Codes/Lot Numbers:

Manufacturing Lot Number and Best Used By 104 12/24/19 105 12/25/19 106 12/26/19 107 12/29/19 110 1/2/20 111 1/3/20 112 1/6/20 114 1/9/20 115 1/10/20 116 1/13/20 117 1/14/20 118 1/15/20 119 1/16/20 120 1/17/20 121 1/20/20 123 1/20/20 124 1/23/20 125 1/24/20 126 1/27/20 127 1/28/20 128 1/29/20 129 1/30/20 130 1/31/20 131 2/3/20 132 2/4/20 133 2/5/20 134 2/6/20 135 2/7/20 136 2/10/20 137 2/12/20

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0501-2020

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