Davol Recalls
8 recalls on record · July 6, 2022 to April 29, 2026 · Medical Devices
Recalls by year
22
23
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 29, 2026Medical DevicesFDA
Davol, Inc. recalls Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm. Catalog Number: 1050030.
Hazard: Potential for product to contain foreign matter, confirmed to be inspect fragments.
August 2, 2023Medical DevicesFDA
Davol, Inc. recalls Ventralight ST w EchoPS 4"x6" Ellipse- A low profile, bioresorbable, coated, permanent mesh, with a pre-attached removab
Hazard: Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequate mesh placement, erosion/migration, pain and mesh infection
August 2, 2023Medical DevicesFDA
Davol, Inc. recalls Ventralight ST w Echo PS 4.5" Circle A low profile, bioresorbable, coated, permanent mesh, with a pre-attached removab
Hazard: Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequate mesh placement, erosion/migration, pain and mesh infection
August 2, 2023Medical DevicesFDA
Davol, Inc. recalls Ventralight ST 4.5" Circle with Echo PS- A low profile, bioresorbable, coated, permanent mesh, with a pre-attached remov
Hazard: Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequate mesh placement, erosion/migration, pain and mesh infection
August 2, 2023Medical DevicesFDA
Davol, Inc. recalls Ventralight ST 4" x 6" Ellipse with Echo PS Catalog Number: 5955460
Hazard: Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequate mesh placement, erosion/migration, pain and mesh infection
August 3, 2022Medical DevicesFDA
Davol, Inc. recalls X-Stream Irrigation System (Catalog No. 5551000) and X-Stream Irrigation System Refurbished (Catalog No. 9551000)
Hazard: The device may potentially cause a fire, leading to a safety risk.
July 6, 2022Medical DevicesFDA
Davol, Inc. recalls HydroSurg Plus Laparoscopic Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, 33cm Tip and Cojoined Suction and Irr
Hazard: The product is not able to provide irrigation.
July 6, 2022Medical DevicesFDA
Davol, Inc. recalls HydroSurg Plus Laparoscopic Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, Handle only, with Cojoined Suction an
Hazard: The product is not able to provide irrigation.