100% CIDER Pasteurized APPLE WEDGE CIDER 1 Gal. (3.78L) HENDERSONVILLE, NC 28792 Keep Refrigerated 0.1% Potassium Sorbat
Summary
The FDA issued a Class II for 100% CIDER Pasteurized APPLE WEDGE CIDER 1 Gal. (3.78L) HENDERSONVILLE, NC 28792 by Apple Wedge LLC. Reason: Patulin. Apple Cider was found to have elevated levels of patulin after receiving analytical testing results from 3rd party laboratory. Lab sample det.
Details
Source
Food Recall
External ID
F-0249-2025
Action Date
2024-12-11
Status
Ongoing
Category
food
Product Description
100% CIDER Pasteurized APPLE WEDGE CIDER 1 Gal. (3.78L) HENDERSONVILLE, NC 28792 Keep Refrigerated 0.1% Potassium Sorbate as Preservative UPC 0 36482 12800 0
Lot/Code Info: C3419 SELL BY 12/09/2024
Quantity Affected: 218 cases (872/128oz containers)
Reason for Recall
Patulin. Apple Cider was found to have elevated levels of patulin after receiving analytical testing results from 3rd party laboratory. Lab sample detected 78 ppb; limit is 50 ppb.
Distribution
Products were shipped to GA, NC, SC and FL.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-07
Company
Hendersonville, NC
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 107 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Apple Wedge LLC has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Apple Wedge LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Apple Wedge LLC have FDA actions?
Apple Wedge LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0249-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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