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Class IITerminated in FDA datasetRecall initiated Jan 14, 2016

Pint Umpqua Dairy Cultured Sour Cream, Item no. 03654, net w. 16 oz.

Recalling firm: Umpqua Dairy Products Co

Why it was recalled

Sour cream was made from milk which was tested presumptive positive for beta lactam antibiotics. The firm did not conduct any confirmation test.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 13, 2016.

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Compare the exact product and package details with the label you have.

ProductPint Umpqua Dairy Cultured Sour Cream, Item no. 03654, net w. 16 oz.; UPC 0 71203 00403 4. Half Pint Umpqua Dairy Cultured Sour Cream, Item no. 03751, net w. 18 oz.; UPC 0 71203 00401 0.
Package size16 oz
UPC071203004010, 071203004034

FDA code information

Sell by 2/5/16

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Pint Umpqua Dairy Cultured Sour Cream, Item no. 03654, net w. 16 oz.; UPC 0 71203 00403 4. Half Pint Umpqua Dairy Cultured Sour Cream, Item no. 03751, net w. 18 oz.; UPC 0 71203 00401 0.

Extracted codes and context

TypeCode / valueContext
UPC071203004010 Half Pint Umpqua Dairy Cultured Sour Cream, Item no. 03751, net w. 18 oz.; UPC 0 71203 00401 0.
UPC071203004034Pint Umpqua Dairy Cultured Sour Cream, Item no. 03654, net w. 16 oz.; UPC 0 71203 00403 4. Half Pint Umpqua Dairy Cultured Sour Cream, Item no. 03751, net w. 18 oz.; UPC 0 71203 00401 0.

Original FDA recall reason

Sour cream was made from milk which was tested presumptive positive for beta lactam antibiotics. The firm did not conduct any confirmation test.

Recall details

Recall number
F-0601-2016
Event ID
73097
FDA status
Terminated
Initiated
Jan 14, 2016
Reported
Feb 24, 2016
Classified
Feb 17, 2016
Terminated
Oct 13, 2016
Quantity
5340/16 oz. cups; 1975/8 oz. cups
Location
Roseburg, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

distributed in AK, ID, CA, MT, OR, and WA.

FDA source record · F-0601-2016

Data updated September 16, 2026. View official FDA data ↗

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