Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1249-2017 — 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 labe

U.S. FDA — Device Enforcement · United States · 2016-11-22 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1249-2017
Date of alert
2016-11-22
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Reckitt Benckiser LLC
Product category
device
Product type
Devices
Reported risk: Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to missing information on the package labeling associated with the active ingredient Benzocaine.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.