Facility

Qingdao London Durex Co., Ltd.

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

Key facts

4recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3008559248
Establishment type	Manufacture Medical Device
Location	No. 1-13 Shangma Part Qingdao Shandong, CN 26611
Registration status	Active · expires 2026
Parent company	Reckitt Benckiser LLC (owner-operator 9004884)
Brand names	Durex Extra Sensitive Smooth; Durex Pleasure Pack; Durex Extra Sensitive Close; Durex Adventure Pack; Durex Air Close Fit; Durex Extra Sensitive Regular; Durex Extra Sensitive Thin; Extra Sensitive Thin Regular Fit

Activity by year

Recalls (4)

Devices registered here (1)

Condom
Product code HIS (opens in a new tab) · Class II · Obstetrics/Gynecology · 21 CFR 884.5300

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. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Qingdao London Durex Co., Ltd. (FEI 3008559248) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3008559248-qingdao-london-durex-co-ltd/

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