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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
1 Event
Recall of Device Recall Bard Deluxe Guidewire PEG
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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
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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
Language
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