INTERGARD Woven Vascular Graft is a woven polyester graft coated with a bovine collagen. It has an external velour surface and non-velour inner surface. The device is available in straight tubes and bifurcated configurations, as well as hemabridge, aortic arch, thoracic aortic graft, and cardioroot configurations designed for use on the thoracic aorta
Reported: June 29, 2022 Initiated: April 29, 2022 #Z-1282-2022
Product Description
INTERGARD Woven Vascular Graft is a woven polyester graft coated with a bovine collagen. It has an external velour surface and non-velour inner surface. The device is available in straight tubes and bifurcated configurations, as well as hemabridge, aortic arch, thoracic aortic graft, and cardioroot configurations designed for use on the thoracic aorta
Reason for Recall
Mislabeled: Product labeled as Intergard Woven Straight graft REF IGW0032-30, D: 8 mm, L: 30 cm, contained an Intergard Woven Straight graft of D: 32 mm and L: 30 cm
Details
- Recalling Firm
- Maquet Cardiovascular, LLC
- Units Affected
- 1 unit
- Distribution
- US Nationwide distribution in the state of SC.
- Location
- Wayne, NJ
Frequently Asked Questions
What product was recalled? ▼
INTERGARD Woven Vascular Graft is a woven polyester graft coated with a bovine collagen. It has an external velour surface and non-velour inner surface. The device is available in straight tubes and bifurcated configurations, as well as hemabridge, aortic arch, thoracic aortic graft, and cardioroot configurations designed for use on the thoracic aorta. Recalled by Maquet Cardiovascular, LLC. Units affected: 1 unit.
Why was this product recalled? ▼
Mislabeled: Product labeled as Intergard Woven Straight graft REF IGW0032-30, D: 8 mm, L: 30 cm, contained an Intergard Woven Straight graft of D: 32 mm and L: 30 cm
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 29, 2022. Severity: Moderate. Recall number: Z-1282-2022.
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