FDA recall record

Bevovations, LLC dba New England Apple Products Apple Cider packed under the following recall — FDA F-2158-2017

Product contains elevated levels of patulin.

Class IIclassification
F-2158-2017official record ID
May 3, 2017report date

Recall record at a glance

Official recordF-2158-2017
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBevovations, LLC dba New England Apple Products Company
Report dateMay 3, 2017
Recall initiation dateMar 28, 2017
Quantity1,409 cases (total for all product)
LocationLeominster, MA, United States

Official product description

Apple Cider packed under the following labels: RUDY'S BLEND APPLE CIDER, 1 GAL. (3.78L), UPC: 8 56005 00344 3; RUDY'S BLEND APPLE CIDER; 1/2 GAL (1.89L), 8 56005 00434 6; FRESHLY PRESSED APPLE CIDER Carlson Orchards Harvard, Mass, 1/2 GAL (1.89L), 8 56005 00323 8; FRESHLY PRESSED APPLE CIDER Carlson Orchards Harvard, Mass, 1 GAL. (3.78 L), 8 56005 00324 5; FRESHLY PRESSED APPLE CIDER Carlson Orchards Harvard, Mass, 16 FL. OZ. (473mL); LYMAN ORCHARDS Pure Sweet Apple Cider, 1 GAL (3.78l), 0 27894 44972 2; LYMAN ORCHARDS Freshly Pressed Apple Cider, 16 OZ (473ml), 0 27894 44672 1

Why the product was recalled

Product contains elevated levels of patulin.

Distribution information

NH, CT, MA, RI

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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