Bonya Pineapple Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 1
Summary
The FDA issued a Class I for Bonya Pineapple Yogurt Parfait, 8oz, Plastic cups with plastic inserts for grano by Knockroe Inc. Reason: Undeclared Almonds.
Details
Source
Food Recall
External ID
F-0770-2025
Action Date
2025-05-21
Status
Ongoing
Category
food
Product Description
Bonya Pineapple Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Lot/Code Info: Pallet Lot #s: 112, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179,180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202,203, 204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216
Quantity Affected: 3912 Units
Reason for Recall
Undeclared Almonds
Distribution
The recalled product was distributed to the following states: NY, PA, MA, NJ.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-03-29
Company
Elizabethtown, PA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 51 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Knockroe Inc has 12 FDA actions in our database, including 12 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Knockroe Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Knockroe Inc have FDA actions?
Knockroe Inc has 12 FDA actions in our database, including 12 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0770-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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