FDA Recall
Terminated
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)
Recall: Z-1249-2017
·
Initiated November 22, 2016
Recall
- Recall Number
- Z-1249-2017
- Event Number
- 75829
- Firm
- Reckitt Benckiser LLC
- FEI Number
- 3011015568
- Product Code
- HIS
- Status
- Terminated
- Root Cause
- Error in labeling
- Initiated
- November 22, 2016
- Terminated
- January 15, 2020
- Address
- 399 Interpace Pkwy, Parsippany, NJ, 07054-1133
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)
Reason
Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to missing information on the package labeling associated with the active ingredient Benzocaine.
Action
Reckitt Benckiser LLC sent an Urgent Medical Device Recall letter/business response form dated November 22, 2016 to the affected customers. Stericylcle is handling returns.
Distribution
Nationwide and Foreign
Quantity
108342 units