FDA Recall United States Terminated Historical recordClass II
Bevovations, LLC dba New England Apple Products Company
- Product
- Apple Cider packed under the following labels: RUDY'S BLEND…
- Published
- May 3, 2017
- Distribution
- Multiple states
Bevovations, LLC dba New England Apple Products Company Recall: Product contains elevated levels of patulin.
United States
TerminatedClass II
- Company
- Bevovations, LLC dba New England Apple Products Company
- Product
- Apple Cider with Potassium Sorbate, packed under the followi…
- Recall date
- March 28, 2017
- Terminated
- July 3, 2017
- Source
- FDA
Reason for recall
Product contains elevated levels of patulin.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Apple Cider with Potassium Sorbate, 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 | Not published in this source record | 1,409 cases (total for all product) | Best By Apr 23 |
Distribution
- NH
- CT
- MA
- RI
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-2157-2017
- Event ID
- 76883
- Status
- Terminated
- Classification
- Class II
- Company
- Bevovations, LLC dba New England Apple Products Company
- Product description
- Apple Cider with Potassium Sorbate, 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
- Quantity
- 1,409 cases (total for all product)
- Reason
- Product contains elevated levels of patulin.
- Recall initiation date
- March 28, 2017
- Report date
- May 3, 2017
- Classification date
- Not published in this source record
- Termination date
- July 3, 2017
- Distribution pattern
- NH, CT, MA, RI
- UPC, lot, and code information
- Best By Apr 23
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 76883 with 1 other product entry in Public Health Trace.
Responsible company: Bevovations, LLC dba New England Apple Products Company
Other recalls from Bevovations, LLC dba New England Apple Products Company
FDA Recall United States Terminated Historical recordClass II
Bevovations, LLC dba New England Apple Products Company
- Product
- Apple Cider packed under the following labels: RUDY'S BLEND…
- Published
- May 3, 2017
- Distribution
- Multiple states
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| New Hampshire | 1 |
| Connecticut | 1 |
| Massachusetts | 1 |
| Rhode Island | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
