Papablic Inc recalls Papablic Replacement Brush Heads. Model Number: PAPA317AA.
Reason for recall
Potential for brush heads to break.
Affected product
Check your device
Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.
Papablic Replacement Brush Heads. Model Number: PAPA317AA.
Lot / code information
- Model
- PAPA317AA; Amazon FNSKU: X0040USQ0N
- Lot #
- PS2509A01, PS2511A01, PS2512A01; Date Codes: 2509, 2511, 2512. The recalled product is limited to PAPA317AA replacement brush head packs bearing the above
- Lot #
- date codes. Products with other
- Lot #
- date codes are not included in this recall
What the firm is doing
Papablic notified their direct customer on about 05/21/2026, who then notified users on about 06/04/2026 electronically. Consignees were instructed of the issue and to immediately stop using the affected replacement brush heads and dispose of them in household trash. Customers will not be required to return the affected product to the firm. The letter provided directs users to Papablic's website where they can file their claim and acknowledge the notification. Customers will be asked to provide proof of purchase and/or product identification information, such as order number, product model, batch code/date code, and photos if available, to confirm eligibility. Eligible customers will be offered a free replacement with updated product or a refund, as applicable.
DistributionShow detailsHide
US Nationwide distribution.
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-2734-2026
- FDA device classification · JEQOfficial FDA classification for this device type
- CFR regulation · 21 CFR 872.6865The federal regulation governing this device
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find Papablic IncSearch for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.
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