Medical device recalls Moderate risk

Reckitt Benckiser LLC recalls Durex Pleasure Pack . 3 ultra fine lubricated latex condoms 12 ultra fine lubricated latex condoms 24 Ra fine lubricate…

Recall date
November 22, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1249-2017
FDA classification
Class II
Brand / firm
Reckitt Benckiser LLC
Sold / distributed
Nationwide and Foreign

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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)

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