Reckitt Benckiser LLC
4 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (4)
Devices registered here (1)
- Orthosis, Corrective ShoeProduct code KNP (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.3475
Recalls & enforcement
- Class IITerminated2018-12-19Five batches of the product have failed the specification of 1.0kPa for Burst Pressure.
- Class IITerminated2018-08-06Product 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 IITerminated2018-07-23The products failed the filed specification of 1.0kPa for Burst Pressure.
- Class IITerminated2016-11-22Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to missing information on the package labeling associated with the active ingredient Benzocaine.
Related
- All facilities operated by Reckitt Benckiser LLC
- Reckitt Benckiser LLC (PA)
- SSL MANUFACTURING (THAILAND) LTD. (TH)
- Reckitt Benckiser Healthcare Manufacturing (Thailand) Ltd. (TH)
- Qingdao London Durex Co., Ltd. (CN)
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Reckitt Benckiser LLC (FEI 3011015568) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3011015568-reckitt-benckiser-llc/
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