Devices

Device Recall Bard PEG

Model / Serial
Lots: 43FQA076, 43IQA096, 43KQA098, HURD1299, HURE3445 , HURI0365, HUSA0502, HUSC0154.
Product Classification
Gastroenterology-Urology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide, including USA, Belgium, Canada, Australia, and Japan.
Product Description
Bard Access Systems, Inc., Bard* PEG (Percutaneous Endoscopic Gastrostomy) Safety System - "Guidewire" , REF 003028, 28F, Sterile.
Manufacturer
C.R. Bard Access Systems, Inc
1 Event
- Recall of Device Recall Bard PEG

Manufacturer

C.R. Bard Access Systems, Inc

Manufacturer Address
C.R. Bard Access Systems, Inc, 5425 Amelia Earhart Dr, Salt Lake City UT 84116-3713
Source
USFDA

2 devices with a similar name

Learn more about the data here

Device Recall Bard PEG

Model / Serial
Lots: 43FQAO78, 43FQA186, 43GQA080, 43HQA083, 43lQA092, 43JQA083,43KQA197, 43LQA202, HURA1457, HURB2555, HURD1301, HURD1995, HURE2973, HURE3447, HURE3448, HURF0572, HURG0273, HURH0036, HURH1222, HURJ0797, HURK1562, HUSA0504, HUSB1435, HUSC0155, HUSD0380, HUSD2072, HUSE0001, HUSF0580.
Product Classification
Gastroenterology-Urology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide, including USA, Belgium, Canada, Australia, and Japan.
Product Description
Bard Access Systems, Inc., Bard* PEG (Percutaneous Endoscopic Gastrostomy) Safety System - "Guidewire" REF 003030, 20F, Sterile.
Manufacturer
C.R. Bard Access Systems, Inc

Device Recall Bard PEG

Model / Serial
Lots: 43DQA032 , 43FQA161, 43GQA068, 43HQA056, 43IQA058, 43JQA059, 43KQA075, 43LQA078, HURA1477, HURB2561, HURD0513, HURD1835, HURE2826, HURF0409, HURG1390, HURH0876, HURJ0544, HURJ0545, HURJ1447, HURJ1448, HUSD0101, HUSD1943, HUSE1509, HUSF1754.
Product Classification
Gastroenterology-Urology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide, including USA, Belgium, Canada, Australia, and Japan.
Product Description
Bard Access Systems, Inc., Bard* PEG (Percutaneous Endoscopic Gastrostomy) Safety System - "Guidewire", REF 006036, 20F, Sterile.
Manufacturer
C.R. Bard Access Systems, Inc

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

Stories in your inbox

Do you work in the medical industry? Or have experience with a medical device? Our reporting is not done yet. We want to hear from you.

Tell us your story!

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.

Download the data

The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

Download all (zipped)