Reckitt Benckiser LLC: Medical Device Recall in 2017 - (Recall #: Z-1249-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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)

Product Classification:

Class II

Date Initiated: November 22, 2016

Date Posted: March 1, 2017

Recall Number: Z-1249-2017

Event ID: 75829

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.

Status: Terminated

Product Quantity: 108342 units

Code Information:

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

Distribution Pattern:

Nationwide and Foreign

Voluntary or Mandated:

Voluntary: Firm initiated