Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bard¿Ventralight" ST Mesh with Echo PS" 10"x13" Reorder Number: 5955113 Recalled by Davol, Inc., Subs. C. R. Bard, Inc. Due to Pouch holding sterile inflation assembly and inflation adapter...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Davol, Inc., Subs. C. R. Bard, Inc. directly.
Affected Products
Bard¿Ventralight" ST Mesh with Echo PS" 10"x13" Reorder Number: 5955113 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.
Why Was This Recalled?
Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Davol, Inc., Subs. C. R. Bard, Inc.
Davol, Inc., Subs. C. R. Bard, Inc. has 20 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report