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Recall archive

94,355 stored notices, from Jun 20, 2012 to Sep 23, 2026.

4 recalls · page 1 of 1

Medical devices

Reported Nov 19, 2014

Bard¿ PerFix Light Plug The Bard¿ PerFix Light Plug is indicated for reinforcement if soft tissue, where weakness…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Davol, Inc., Subs. C. R. Bard, Inc.

Matched: Brand · Product · Product details · Reason for recall — 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…

FDA (openFDA device enforcement)

Medical devices

Reported Jun 11, 2014

Composix" LP with Echo PS" 10x13 HUXH0294 HUXL0314 Indicated for use in the reconstruction of soft tissue deficiencies,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Davol, Inc., Subs. C. R. Bard, Inc.

Matched: Brand — Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2014

Composix L/P with Echo PS 10" X 13" Product Code 0144113 The Composix L/P Mesh with Echo PS Positioning System is a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Davol, Inc., Subs. C. R. Bard, Inc.

Matched: Brand — Product labeling does not match product configuration.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 26, 2012

Bard Ventralight ST Mesh. - Ellipse 8" x 10" (20.3 cm x 25.4 cm) Product Code 5954810. The Bard Ventralight ST Mesh is…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Davol, Inc., Subs. C. R. Bard, Inc.

Matched: Brand · Product · Product details — 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

1 more product in this recall

FDA (openFDA device enforcement)

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