International Medical Devices Database

Manufacturer Address
Taut, Inc., 2571 Kaneville Ct, Geneva IL 60134-2505
Source
USFDA
1 Event
- Recall of Device Recall Taut Intraducer Peritoneal Catheter

One device in the database

Device Recall Taut Intraducer Peritoneal Catheter

Model / Serial
catalog number (REF) PI-128, lot number 04116, use by 2008-01, and lot number 05178, use by 2008-09 These two lots of catheters were sold individually and as sterile components of catalog number (REF) 50000, kit lot numbers KC05107, KC05186, KC06002, KC06025, KC06071, KC06060, KC06087, KC06116
Product Classification
General and Plastic Surgery Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide, including USA, Guam, Australia, Iceland and Italy
Product Description
Taut Intraducer Peritoneal Catheter, 12 Fr x 10 Fr x 20.3 cm; a sterile, Rx peritoneal catheter for single use, individually packaged in a Tyvek/clear pouch; Taut Inc., 2561 Kaneville Ct., Geneva, IL 60134; the individually packaged, sterilirzed catheter was sold in two configurations: || a) catalog number (REF) P.I.-128: 10 catheters per box, 10 boxes per case, and || b) a sterile component of the convenience kit, catalog number (REF) 50000, System One Comprehensive Lap CBDE Kit

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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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Taut, Inc.

One device in the database

Device Recall Taut Intraducer Peritoneal Catheter