Hiland 100% Pure Apple Juice From Concentrate No Sugar Added Pasteurized 4 FL OZ (118 mL) packaged in paper cartons 75 c
Summary
The FDA issued a Class II for Hiland 100% Pure Apple Juice From Concentrate No Sugar Added Pasteurized 4 FL OZ by Hiland Dairy Foods Company LLC. Reason: Elevated levels of inorganic arsenic..
Details
Source
Food Recall
External ID
F-0879-2021
Action Date
2021-09-01
Status
Terminated
Category
food
Product Description
Hiland 100% Pure Apple Juice From Concentrate No Sugar Added Pasteurized 4 FL OZ (118 mL) packaged in paper cartons 75 cartons per case
Lot/Code Info: Best By Date: 07/15/21, 07/17/21, 07/18/21, 07/24/21,07/25/21, 07/29/21, 07/31/21, 08/04/21, 08/05/21, 08/07/21, 08/08/21
Quantity Affected: 436,884 4 oz units
Reason for Recall
Elevated levels of inorganic arsenic.
Distribution
AR, MO, KS, OK, TX
Type: Voluntary: Firm initiated
Recall Initiated: 2021-07-22
Company
Springfield, MO
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 40 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Hiland Dairy Foods Company 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 (Hiland Dairy Foods Company LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Hiland Dairy Foods Company LLC have FDA actions?
Hiland Dairy Foods Company 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-0879-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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