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AROA Biosurgery Recalls
24 recalls on record · November 14, 2018 to November 21, 2018 · Medical Devices
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex 2S Reinforced BioScaffold 10x12cm, Part Number F10258-1012G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex Reinforced BioScaffold 18x22cm, Part Number F10254-1822G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex 2S Reinforced BioScaffold 20x20cm, Part Number F10258-2020G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex 2S Reinforced BioScaffold 18x22cm, Part Number F10258-1822G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex 2S Reinforced BioScaffold 16x20cm, Part Number F10258-1620G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex 2S Reinforced BioScaffold 10x20cm, Part Number F10258-1020G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex 2S Reinforced BioScaffold 10x12cm, Part Number F10258-1012G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex 2S Reinforced BioScaffold 6x10cm, Part Number F10258-0610G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex 1S Reinforced BioScaffold 20x20cm, Part Number F10256-2020G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex 1S Reinforced BioScaffold 18x22cm, Part Number F10256-1822G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex 1S Reinforced BioScaffold 16x20cm, Part Number F10256-1620G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex 1S Reinforced BioScaffold 10x20cm, Part Number F10256-1020G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex 1S Reinforced BioScaffold 10x12cm, Part Number F10256-1012G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex 1S Reinforced BioScaffold 6x10cm, Part Number F10256-0610G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex 1S Reinforced BioScaffold 4x8cm, Part Number F10256-0408G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex Reinforced BioScaffold 20x20cm, Part Number F10254-2020G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex Reinforced BioScaffold 16x20cm, Part Number F10254-1620G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex Reinforced BioScaffold 10x20cm, Part Number F10254-1020G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex Reinforced BioScaffold 10x12cm, Part Number F10254-1012G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex Reinforced BioScaffold 6x10cm, Part Number F10254-0610G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 21, 2018Medical DevicesFDA
AROA Biosurgery, LTD. recalls OviTex Reinforced BioScaffold 4x8cm, Part Number F10254-0408G
Hazard: Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that devices over 18-months showed evidence of no longer meeting the pre-defined ball burst specification respective to the number of tissue layers.
November 14, 2018Medical DevicesFDA
AROA BIOSURGERY recalls Endoform Dermal Template 4x5, SKU 529313 Product Usage: Endoform Dermal Template is a sterile, single use ovine fore
Hazard: Potential for pouch seal failure
November 14, 2018Medical DevicesFDA
AROA BIOSURGERY recalls Endoform Dermal Template 2x2, SKU 529312 Product Usage: Endoform Dermal Template is a sterile, single use ovine fore
Hazard: Potential for pouch seal failure
November 14, 2018Medical DevicesFDA
AROA BIOSURGERY recalls Endoform Dermal Template 2x2, SKU 529311 Product Usage: Endoform Dermal Template is a sterile, single use ovine fore
Hazard: Potential for pouch seal failure