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DUREX Tropical Apple

RB Health (us) LLC · Model Condom · UDI-DI 00302340856416

HIS
1
510(k) clearances
408
Adverse events (3 deaths)
7
Recalls
77
Facilities

Description

Condom

Recalls

DateFirmReason
2025-12-26GOLD STAR DISTRIBUTION INCPotential exposure of rodents and rodent activity in the distribution center.
2022-06-23Family Dollar Stores, Llc.Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
2016-11-22Reckitt Benckiser LLCReckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to missing information on the package labeling associated with the active ingredient Benzocaine.
2013-01-14Ansell Healthcare Products LLCOut of an abundance of caution, Ansell is implementing a voluntary recall of the Zero Latex Condom (regular) product. The condom has met or exceeded test and quality standards req
2012-11-05Ansell Healthcare Products LLCOne lot of Lifestyles Pleasure Collection Lubricated Condoms is misbranded. Ultra Thin was included rather than Skyn.
2007-09-11Global Protection Corp.Condoms fail the water leak test and package integrity
2002-11-25Ansell Healthcare IncThe condoms are being recalled because information recently available indicates some of these condoms do not meet airburst test standards

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.