CLASS II Device recall · Reported 1 Mar 2017 · FDA Enforcement Report

Durex Pleasure Pack . 3 ultra fine lubricated latex condoms recalled

Reckitt Benckiser is recalling Durex Pleasure Pack . 3 ultra fine lubricated latex condoms 12 ultra fine lubricated, distributed nationwide in the US. The recall was initiated on 22 Nov 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes3ct - item code 02340-30042-04 lot code exp date 3 ct - Walmart item code 02340-70042-04 lot code exp date 12ct - item code 02340-30274-08 lot code exp date 24 ct - item code 02340-302190-04 lot codes and exp date

Quantity recalled108342 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1249-2017
FDA event ID: 75829
Recalling firm: Reckitt Benckiser, Parsippany, NJ
Classification: Class II
Status: Terminated
Recall initiated: 22 Nov 2016
FDA classified: 23 Feb 2017
Reported: 1 Mar 2017
Type: Voluntary: Firm initiated
Customers notified by: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category: Labeling Errors
Device type: Other Medical Devices

Timeline

22 Nov 2016	Recall initiated by company
23 Feb 2017	Classified by FDA	+93 days
1 Mar 2017	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to missing information on the package labeling associated with the active ingredient Benzocaine.

Product as listed by the FDA

Durex Pleasure Pack . 3 ultra fine lubricated latex condoms 12 ultra fine lubricated latex condoms 24 Ra fine lubricated latex condoms 3 ct UPC 3-02340-30042-04-1 3 ct - Walmart UPC 02340-70042-04 12ct - UPC 3-02340-30274-08-6 24 ct - UPC 302340-302190-04 (contacting firm for label)

Where it was distributed

Nationwide and Foreign

Nationwide

Stores named: Walmart

Questions about this recall

Why was it recalled?

Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to missing information on the package labeling associated with the active ingredient Benzocaine.

Which lots are affected?

3ct - item code 02340-30042-04 lot code exp date 3 ct - Walmart item code 02340-70042-04 lot code exp date 12ct - item code 02340-30274-08 lot code exp date 24 ct - item code 02340-302190-04 lot codes and exp date

Where was it sold?

Nationwide and Foreign

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Reckitt Benckiser

All 15

Reported	Class	Recall	Company	Reason	Where
20 Mar 2019Device	CLASS II	Durex Real Feel, synthetic polisoprene male condom recalled	Reckitt Benckiser	Other	Nationwide
20 Mar 2019Device	CLASS II	Durex Pleasure Pack, synthetic polisoprene male condom recalled	Reckitt Benckiser	Other	Nationwide
17 Oct 2018Device	CLASS II	Polyisoprene condomns recalled by Reckitt Benckiser	Reckitt Benckiser	Device Malfunction	NY
3 Oct 2018Device	CLASS II	Durex Real Feel Polyisoprene Condoms recalled by Reckitt Benckiser	Reckitt Benckiser	Other	Nationwide
28 Sep 2016Drug	CLASS III	Mucinex Sinus-Max Day Night, 60 caplets recalled by Reckitt Benckiser	Reckitt Benckiser	Other	FL, MA, NJ

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