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Class IIFDA · August 12, 2026

Pumpkin Tree Peter Rabbit Organics Banana & Strawberry recall

Recalled by PT Organics Limited

The product, as the FDA describes it: Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree, 4oz/113g pouch, UPC 815367010780, PTO Item 10720. Distributed by: PT Organics Ltd, 333 South State St, Suite V-142, Lake Oswego, OR 97034. Product is pasteurized blend of banana and strawberry purees sold in single serve spouted flexible film pouch (4oz/113g) with red cap. It is intended for consumption by children aged +6 months. Each master case contains 10/4oz. pouches of PT Organics Banana Strawberry 1006034. The bar code on master case label is 00815367010797.

Why it was recalled

Possible foreign object (thin, soft plastic strands).

What to do if you have it

Something physical ended up in the product, so the risk is injury rather than illness, and it is uneven: some packages carry it and most do not. That makes the lot codes below the whole decision. Do not pick through pumpkin tree peter rabbit organics banana & strawberry to check it yourself.

How to tell whether your package is one of them

A recall covers particular production runs, not everything the company makes, so the codes decide it. These are the ones the FDA published. Match them against what is printed on your package, usually near the best-before date.

Production lane number and Best By Dates on 4oz/113g pouches: Number "4" on the yellow right seam on the back of the pouch which indicates the packaging production lane 4. Best By Dates (BB): 01/19/2027 01/20/2027 03/17/2027 03/18/2027 05/14/2027 05/15/2027 LOT CODES printed on MASTER CASE (10 pouches/ case): 260119, 260120, 260317, 260318, 260514, 260515

The details on record

Recalling companyPT Organics Limited
Company locationLake Oswego, OR
Where it was distributedDistributed in AL, AZ, CA, CO, GA, IA, IL, IN, KS, MI, MN, NC, NJ, NY, OH, OR, PA, SC, TN, TX, VA, WA, and WI.
How much was recalled4,385 (4-oz units) of defective pouches from total lot produced
Recall startedJuly 13, 2026
Published by the FDAAugust 12, 2026
Recall typeVoluntary: Firm initiated
How the company announced itTwo or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA recall numberH-1223-2026

Everything above comes from the FDA enforcement report for this recall. Read the official notice for the company's own wording, contact numbers, and any photographs of the packaging.

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