Flexible food pouch (3-layer foil, spouted, #CP6088), manufactured for packaging Pumpkin…
CHEER PACK recalled this product and the FDA reported the enforcement action on 12 August 2026 as Class II. The recall was initiated by the firm. Flexible food pouch may release thin plastic strips into food.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Flexible food pouch (3-layer foil, spouted, #CP6088), manufactured for packaging Pumpkin Tree Peter Rabbit Organics Banana & Strawberry, 4 oz food puree, UPC 815367010780.
- UPC
- 815367010780
- Reason for recall
- Flexible food pouch may release thin plastic strips into food.
- Recalling firm
- CHEER PACK
- Firm location
- West Bridgewater, Massachusetts, United States
- Classification
- Class II
- Status
- Ongoing
- Recall number
- H-1193-2026
- Quantity
- 322,450 (4 oz) units
- Distribution
- only in OR.
- Initiated
- 16 July 2026
- Reported by FDA
- 12 August 2026
- Firm notified by
- Product codes
- Food pouch (3-layer foil, spouted, Cheer Pack Part#CP6088) manufactured for packaging food products. Customer Part #31720. Manufacture date 10/25/25 - 10/31/25. Lot Numbers: LSS20100005297, LSS2010000598, LSS20100005300, LSS20100005301, LSS 20100005302, LSS20100005303, LSS20100005304, LSS2015306, LSS20100005307, LSS20100005308, LSS20100005309, LSS20100005310.
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This record is the only one the FDA opened for its recall event, so it covers a single product code.
- This recall has no termination date on the record, so as published it had not been terminated under 21 CFR 7.55.
- The FDA published the enforcement report 4 weeks after the firm began the recall.
- Fresh produce is the category where contamination arrives before the facility does: irrigation water, soil amendments and field workers are the routes, and nothing downstream of the farm is a kill step for a product eaten raw.
What this recall was for
Foreign material
A foreign material recall means something that is not food was found in food: metal, plastic, glass, wood or insect matter, usually shed by equipment during processing.
A preventive controls plan covers foreign material under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.40
- Equipment and utensils: plant equipment designed and maintained so it cannot contaminate food with lubricants, fuel, metal fragments or contaminated water.
- 21 CFR 117.80(c)
- Manufacturing operations: the measures that protect food from contamination during processing, including the effective ones against metal and other extraneous material.
- 21 CFR 117.150
- Corrective actions: what a facility does when a preventive control was not properly implemented, including identifying and correcting the problem and evaluating the food for safety.
Filed under fresh produce. A product can sit in more than one.
Other fresh produce recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
All 2026 recalls · All FDA food recall data
21 CFR 117.40 is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.