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Class II: temporary or reversible health riskTerminated

Contoocook Creamery Butter Recall

Butter (salted)

Contoocook Creamery · Contoocook, NH

Risk level
Class II
Reported by FDA
Sep 11, 2013
Recall ID
F-1859-2013
Check your lot numberHow we source this data

Summary

Contoocook Creamery recalled Butter starting May 17, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1859-2013 on Sep 11, 2013. Reason: Elevated coliform and standard plate count. Status: Terminated.

Why it was recalled

Elevated coliform and standard plate count.

Product description

Butter (salted). 8oz round clear plastic tub and 5 gallon pail. UPC Code 7 93573 09802 3.

Lot numbers, UPCs & expiration codes

N/A

Where it was sold

NH only. No foreign distribution.

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-1859-2013
Classification
Class II
Status
Terminated
Recall initiated
May 17, 2013
FDA report date
Sep 11, 2013
Quantity
quantity unknown
Recall type
Voluntary: Firm initiated
Recalling firm
Contoocook Creamery

Original FDA data

Every field from FDA enforcement report F-1859-2013, exactly as published.

Show all FDA fields
City
Contoocook
State
NH
Status
Terminated
Country
United States
Event ID
65325
Address
945 Penacook Rd
Postal code
03229-3030
Report date
Sep 11, 2013
Product type
Food
Recall number
F-1859-2013
Classification
Class II
Recalling firm
Contoocook Creamery
Product quantity
quantity unknown
Termination date
Apr 14, 2016
Reason for recall
Elevated coliform and standard plate count.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Butter (salted). 8oz round clear plastic tub and 5 gallon pail. UPC Code 7 93573 09802 3.
Distribution pattern
NH only. No foreign distribution.
Recall initiation date
May 17, 2013
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Sep 5, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1859-2013, published Sep 11, 2013. View the source record (openFDA) · FDA enforcement reports

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

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