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Davol, Inc., Subs. C. R. Bard Recalls
20 recalls on record · September 26, 2012 to November 19, 2014 · Medical Devices
Recalls by year
12
14
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
November 19, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard¿ PerFix Light Plug The Bard¿ PerFix Light Plug is indicated for reinforcement if soft tissue, where weakness e
Hazard: The patient record peel-off label product code and size did not match the other labeling and actual product in the packaging for the Bard Small PerFix Light Plug.
June 11, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard¿ Ventralight" ST Mesh with Echo PS" 8"x10" Reorder Number: 5955810 Indicated for use in the reconstruction of s
Hazard: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
June 11, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard¿ Ventralight" ST Mesh with Echo PS" 8" Circle Number: 5955800 Indicated for use in the reconstruction of soft t
Hazard: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
June 11, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard¿ Ventralight" ST Mesh with Echo PS TM 7"x9" Reorder Number: 5955790 Indicated for use in the reconstruction of
Hazard: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
June 11, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard¿ Ventralight" ST Mesh with Echo PS" 6"x8" Reorder Number: 5955680 Indicated for use in the reconstruction of so
Hazard: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
June 11, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard¿ Ventralight" ST Mesh with Echo PS" 6"x10" Reorder Number: 5955610 Indicated for use in the reconstruction of s
Hazard: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
June 11, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard¿ Ventralight" ST Mesh with Echo PS" 6" CircleReorder Number: 5955600 Indicated for use in the reconstruction of
Hazard: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
June 11, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard¿ Ventralight" ST Mesh with Echo PS" 4"x6" Reorder Number: 5955460 Indicated for use in the reconstruction of so
Hazard: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
June 11, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard¿ Ventralight" ST Mesh with Echo PS" 4.5" Circle Reorder Number: 5955450 Indicated for use in the reconstruction
Hazard: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
June 11, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard¿ Ventralight" ST Mesh with Echo PS" 12"x14" Reorder Number: 5955124 Indicated for use in the reconstruction of
Hazard: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
June 11, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard¿Ventralight" ST Mesh with Echo PS" 10"x13" Reorder Number: 5955113 Indicated for use in the reconstruction of s
Hazard: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
June 11, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard¿ Composix" LIP Mesh with Echo PS" 8"x10" Reorder Number: 0144810 Indicated for use in the reconstruction of sof
Hazard: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
June 11, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard¿ Composix" LIP Mesh with Echo PS" 7"x9" Reorder Number: 0144790 Indicated for use in the reconstruction of soft
Hazard: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
June 11, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Composix" LP with Echo PS" 6 x8 Reorder Number: 0144680 Indicated for use in the reconstruction of soft tissue defi
Hazard: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
June 11, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Composix" LP with Echo PS" 6x10 Reorder Number: 0144610 Indicated for use in the reconstruction of soft tissue defic
Hazard: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
June 11, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Composix" LP with Echo PS" 10x13 HUXH0294 HUXL0314 Indicated for use in the reconstruction of soft tissue deficienci
Hazard: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
January 29, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Composix L/P with Echo PS 6" X 8" Product Code 0144680 The Composix L/P Mesh with Echo PS Positioning System is a non
Hazard: Product labeling does not match product configuration.
January 29, 2014Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Composix L/P with Echo PS 10" X 13" Product Code 0144113 The Composix L/P Mesh with Echo PS Positioning System is a n
Hazard: Product labeling does not match product configuration.
September 26, 2012Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard Ventralight ST Mesh. - Ellipse 7" x 9" (17.8 cm x 22.9 cm) Product Code 5954790. The Bard Ventralight ST Mesh
Hazard: Mislabeled: The 8" x 10" package contains 7" x 9" VENTRALIGHT ST Mesh product and the 7" x 9" package contains 8" x 10" VENTRALIGHT ST Mesh
September 26, 2012Medical DevicesFDA
Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard Ventralight ST Mesh. - Ellipse 8" x 10" (20.3 cm x 25.4 cm) Product Code 5954810. The Bard Ventralight ST Mes
Hazard: Mislabeled: The 8" x 10" package contains 7" x 9" VENTRALIGHT ST Mesh product and the 7" x 9" package contains 8" x 10" VENTRALIGHT ST Mesh product