Devices

Device Recall Durex

Model / Serial
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
Product Classification
Obstetrical and Gynecological Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide and Foreign
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)
Manufacturer
Reckitt Benckiser LLC
1 Event
- Recall of Device Recall Durex

Manufacturer

Reckitt Benckiser LLC

Manufacturer Address
Reckitt Benckiser LLC, 399 Interpace Pkwy, Parsippany NJ 07054-1133
Manufacturer Parent Company (2017)
Reckitt Benckiser Group Plc
Source
USFDA

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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