Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 2 Device Recall Papablic

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
 Class 2 Device Recall Papablicsee related information
Date Initiated by FirmMay 21, 2026
Date PostedJuly 15, 2026
Recall Status1 Open3, Classified
Recall NumberZ-2734-2026
Recall Event ID 98898
Product Classification Toothbrush, powered - Product Code JEQ
ProductPapablic Replacement Brush Heads. Model Number: PAPA317AA.
Code Information Model Number: PAPA317AA; Amazon FNSKU: X0040USQ0N; Lot Numbers: PS2509A01, PS2511A01, PS2512A01; Date Codes: 2509, 2511, 2512. The recalled product is limited to PAPA317AA replacement brush head packs bearing the above lot numbers/date codes. Products with other lot numbers/date codes are not included in this recall.
FEI Number 3045522789
Recalling Firm/
Manufacturer		 Papablic Inc
2146b S Archer Ave
Chicago IL 60616-1514
Manufacturer Reason
for Recall		Potential for brush heads to break.
FDA Determined
Cause 2		Device Design
ActionPapablic 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.
Quantity in Commerce13,400 packs
DistributionUS Nationwide distribution.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
-
-