Summary
The FDA issued a Class II for Papablic Replacement Brush Heads. Model Number: PAPA317AA. by Papablic Inc. Reason: Potential for brush heads to break..
Details
Source
Device Recall
External ID
Z-2734-2026
Action Date
2026-07-22
Status
Ongoing
Category
device
Product Description
Papablic Replacement Brush Heads. Model Number: PAPA317AA.
Lot/Code Info: 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.
Quantity Affected: 13,400 packs
Reason for Recall
Potential for brush heads to break.
Distribution
US Nationwide distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-21
Company
Chicago, IL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 102 device recalls issued in the same week, part of 365 device-related FDA actions this month.
Papablic Inc has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Papablic Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Papablic Inc have FDA actions?
Papablic Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-2734-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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