Devices

Device Recall Bard Deluxe Guidewire PEG

Model / Serial
Lots: HURL0217, HUSB0186, HUSC0157, HUSD0382, HUSD2075.
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* Deluxe Guidewire PEG (Percutaneous Endoscopic Gastrostomy) System with Soft Silicone Retention Dome, REF 000628, 20F.
Manufacturer
C.R. Bard Access Systems, Inc
1 Event
- Recall of Device Recall Bard Deluxe Guidewire 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

One device with a similar name

Learn more about the data here

Device Recall Bard Deluxe Guidewire PEG

Model / Serial
Lots: 43DQA112, 43EQA079, 43EQA080, 43FQA074, 43FQA097, 43GQA075, 43GQA076, 43GQA194, 43HQA079, 43HQA080, 43IQA180, 43KQA114, 43KQA115, 43LQA107.
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* Deluxe Guidewire PEG (Percutaneous Endoscopic Gastrostomy) System with Soft Silicone Retention Dome, Sterile, Rx only, REF 000793, 20F.
Manufacturer
C.R. Bard Access Systems, Inc

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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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