Papablic Replacement Brush Heads Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Papablic Inc is recalling 14,700 packs of Papablic Replacement Brush Heads due to potential breakage.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 10, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Papablic Inc has initiated a voluntary recall of certain Papablic Replacement Brush Heads because of the potential for brush heads to break.
Which Products Are Affected
The recall involves Papablic Replacement Brush Heads, Model Number: Papablic18B. Affected products are limited to packs with Amazon FNSKU: X004LOZKE3 and Lot Numbers: PS2509A01, PS2511A01, PS2512A01 (Date Codes: 2509, 2511, 2512). A total of 14,700 packs are affected under recall number Z-2733-2026. Distribution was nationwide in the United States.
What You Should Do
Consumers should verify if their product matches the recalled lot numbers and date codes listed.
Why This Matters
This Class II recall addresses a defect that could lead to product failure during use.
Source
FDA recall Z-2733-2026, event ID 98898. https://www.fda.gov
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (839 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 10, 2026.
Frequently Asked Questions
Common questions about this FDA recall.