RECALL DATABASE

PT Organics Limited Pumpkin Tree Banana & Strawberry puree 4oz pouch Recall (January 2027)

Announced 2026-08-12 · FDA

FDA is recalling PT Organics Limited Pumpkin Tree Banana & Strawberry puree pouches due to a possible foreign object (thin, soft plastic strands). About 4,385 defective 4-oz pouches from this lot were distributed across multiple states. The recall notes production lane 4 and specific Best By dates (01/19/2027, 01/20/2027, 03/17/2027, 03/18/2027, 05/14/2027, 05/15/2027) and master-case LOT codes (260119, 260120, 260317, 260318, 260514, 260515).

BrandPT Organics Limited
ProductPumpkin 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.
ReasonPossible foreign object (thin, soft plastic strands).
Severitymoderate
Units affected4385
DistributionDistributed 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.
AgencyFDA
Recall / campaign no.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

WHAT YOU SHOULD DO

  1. Do not use recalled pouches; discard them.
  2. If you have any recalled pouches, check for production lane 4 on the back seam and the listed Best By dates or the master-case LOT codes; if matched, discontinue use.
  3. Contact PT Organics Limited for a refund or replacement and follow any FDA guidance or instructions from the company.

This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.