RegWardenFDA facility compliance records
Company

Reckitt Benckiser LLC

4 recall(s) on record — most severe on record: Class II.

Recalls by year

FDA actions on record by year2016: 1 recalls; 2018: 3 recalls1201620173201820192020202120222023202420252026
  • Recalls (4)

Registered facilities (5)

Recalls & enforcement

  • Class IITerminated2018-12-19
    Five batches of the product have failed the specification of 1.0kPa for Burst Pressure.
  • Class IITerminated2018-08-06
    Product marketed in U.S. does not have sufficient data to ensure that it will meet the internal burst pressure specifications at the end of 5 yrs shelf-life
  • Class IITerminated2018-07-23
    The products failed the filed specification of 1.0kPa for Burst Pressure.
  • Class IITerminated2016-11-22
    Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to missing information on the package labeling associated with the active ingredient Benzocaine.

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. “Reckitt Benckiser LLC — 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-9004884-reckitt-benckiser-llc/

Not open yet

Alerts for Reckitt Benckiser LLC

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.

Planned

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.