Myers Cider Mill, LLC Recall: Myers Cider Mill LLC, of Monroeville, Ohio has issued a voluntary recall of apple cider due to a process deviation.
United States
TerminatedClass II
- Company
- Myers Cider Mill, LLC
- Product
- 100% APPLE CIDER 1 Gallon (3.78L) UV TESTED KEEP REFRIGERATE…
- Recall date
- October 19, 2016
- Terminated
- January 17, 2020
- Source
- FDA
Reason for recall
Myers Cider Mill LLC, of Monroeville, Ohio has issued a voluntary recall of apple cider due to a process deviation.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 100% APPLE CIDER 1 Gallon (3.78L) UV TESTED KEEP REFRIGERATED UPC 0 85591 00128 1 | Not published in this source record | 200 gallons | All products with press dates between 9/1/16 - 10/15/16 |
Distribution
- Product was only sold in OH
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1954-2017
- Event ID
- 75515
- Status
- Terminated
- Classification
- Class II
- Company
- Myers Cider Mill, LLC
- Product description
- 100% APPLE CIDER 1 Gallon (3.78L) UV TESTED KEEP REFRIGERATED UPC 0 85591 00128 1
- Quantity
- 200 gallons
- Reason
- Myers Cider Mill LLC, of Monroeville, Ohio has issued a voluntary recall of apple cider due to a process deviation.
- Recall initiation date
- October 19, 2016
- Report date
- April 19, 2017
- Classification date
- Not published in this source record
- Termination date
- January 17, 2020
- Distribution pattern
- Product was only sold in OH
- UPC, lot, and code information
- All products with press dates between 9/1/16 - 10/15/16
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Myers Cider Mill, LLC
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 |
|---|---|
| Ohio | 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.
