Community Products, LLC dba Rifton Equipment
2 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (2)
Registered facilities (3)
- Community Products, LLC FEI 3010761454 · PA
- Community Products, LLC FEI 1319061 · NY
- COMMUNITY PRODUCTS, LLC FEI 1000120230 · NY
Recalls & enforcement
- Class IIOngoing2025-12-18Potential for fraying on the body support strap.
- Class IITerminated2019-03-21A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “Community Products, LLC dba Rifton Equipment — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-1319061-community-products-llc-dba-rifton-equipm/
Alerts for Community Products, LLC dba Rifton Equipment
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.