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Home > News > Incident Analysis > HARPPA Playpen Recall: Loose Screws Pose a Choking Risk
Oct.2026 31

HARPPA Playpen Recall: Loose Screws Pose a Choking Risk

Introduction
Canada's May 14 recall covers HARPPA PP04 playpen gates with detachable screws. Check the affected lots, replacement process and caregiver handover.
Details

Health Canada's May 14, 2026 recall notice warns that screws on the HARPPA Wooden Baby Playpen Gate can loosen and detach, creating choking and injury hazards for children.

Conceptual illustration of parents reviewing a Canadian playpen recall while an unused wooden enclosure is set aside
Conceptual recall-check illustration. The adults and wooden prop are fictional; the prop is not an identification image of the recalled HARPPA model.

Match the model and lot, then follow the remedy

The official Health Canada notice, RA-82067, describes an expandable enclosure 24 inches tall. Check the product's model and lot label against these identifiers. The generic enclosure in our illustrations is not an identification image of the recalled model.

Model PP04
Affected lots 2409200385
2412150360
2503080364
Canadian sales period October 2024 to May 2025

The company reported 473 affected units sold in Canada. The notice records four incident reports and no reported injuries in Canada as of May 10, 2026. It does not describe those four reports as four confirmed choking events.

Stop using the recalled product immediately and contact HARPPA for a replacement playpen gate. The notice provides contact details and says recalled products cannot be sold or given away in Canada.

FITIGER safety analysis: loose household hardware

Household hardware belongs in a small-parts hazard check. A screw that separates from a larger item can reach a child just as a loose toy part can. Here, the notice identifies screws that may loosen and detach. This analysis uses that published account and does not establish why the fasteners loosened.

Counting screws or finding them tight today does not satisfy the recall remedy. An affected unit must stay out of use while the replacement is arranged. Do not improvise a repair. Buying an anti choking device would leave the enclosure's detachable-parts hazard in place.

A fictional parent records a model and lot label while checking a product recall on a tablet
A conceptual identification check. Read the actual product label and official notice; the generic paper and screen shown here are not recall documents.

Make sure the next caregiver knows

Before another caregiver takes over, identify the recalled item and explain why it must stay out of use. Keep children away from it. An unused item without an explanation could be mistaken for equipment that is ready to use.

Keep the model and lot details with the replacement correspondence. If the gate moves between family homes, tell both households and check who might bring it back into use. These are FITIGER's suggested planning steps, not findings from a field study.

Emergency preparation has to fit the child

Take current Canadian first-aid training for the child's age before an emergency. Heart & Stroke released Canada's 2025 CPR and emergency cardiovascular care guidelines on October 22, 2025. The AHA's 2025 update explains that infant choking care differs from care for older children and adults; abdominal thrusts are not recommended for infants. For a choking emergency, call 9-1-1 and follow dispatcher instructions while providing appropriate first aid. Do not delay care to find equipment. A choking rescue device does not replace first-aid training.

An April 22, 2025 entry attributed to Alex LeBegue of Ottawa in FITIGER's public customer feedback describes keeping a compact unit in a kitchen drawer. For household planning, the question is whether every caregiver knows where the kit is. That account describes a storage choice. It does not report a rescue or verify that the drawer meets any particular model's storage instructions.

Fictional adult caregivers discuss a written household recall note and an emergency-contact list
A conceptual caregiver handover. No actual customer, incident, child or rescue device is depicted.

What the FAC02 usability report covers

Our public FAC02 human-factors summary describes a completed evaluation involving 30 people: 15 lay rescuers and 15 healthcare professionals. The simulated tasks included preparation, mask selection and installation, device handling and activity after use. The summary concerns how people interacted with equipment. It does not establish a clinical rescue-success rate or show that a device removed a loose screw from a child's airway.

The FAC02 report lists children under one year as a contraindication. A baby-product recall does not make that model suitable for infants. If researching a suction device for choking for an eligible family member, check that model's age limits, instructions and Canadian regulatory status. FITIGER's FoldPumpVac home kit and EasyPumpVac travel kit are different products to research when comparing a portable choking rescue device. Neither link establishes suitability for infants. FITIGER sells both products.

Keep the recalled gate out of use while arranging the replacement. Separately, make sure caregivers' first-aid training is current.