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

FDA recalling firm · 4 enforcement events · 20 product records · 2012–2014 · RI

Davol, Inc., Subs. C. R. Bard, Inc. has 4 FDA enforcement events on this register (20 product records) between 2012 and 2014: 4 device; the busiest year was 2014 with 3.

0% of its events are Class I; the most common class is Class II (4). 0 events are listed as ongoing; the recalling firm's address is in RI.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

Initiated	Product (first record)	Type	Class	Records	Status
8 Oct 2014	Bard¿ PerFix Light Plug The Bard¿ PerFix Light Plug is indicated for reinforcement if soft tissue, where weakness exists, in procedures involving soft tissue repair, such as groin hernia defects.	Device	Class II	1	Terminated
24 Apr 2014	Composix" LP with Echo PS" 10x13 HUXH0294 HUXL0314 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.	Device	Class II	15	Terminated
3 Jan 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 non-absorbable sterile lightweight mesh prosthesis, with a preattached removable positioning system. This system is indicated and designed for the reconstruction of soft tissue deficiencies during…	Device	Class II	2	Terminated
4 Sep 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 a dual-component (absorbable and nonabsorbable) sterile prosthesis. The device classification name is "Mesh, Surgical, Polymeric." It is in tented for use in the reconstruction of soft tissue…	Device	Class II	2	Terminated

By type and class

Device4

Class II4

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

Enforcement events for Davol, Inc., Subs. C. R. Bard, Inc. by year initiated.

Questions and answers

How many FDA recalls has Davol, Inc., Subs. C. R. Bard, Inc. had?

4 enforcement events (20 product records) on this register, 2012–2014: 4 device.

Are any Davol, Inc., Subs. C. R. Bard, Inc. recalls ongoing?

0 events are listed as ongoing in the current openFDA export.

What class are Davol, Inc., Subs. C. R. Bard, Inc. recalls?

4 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.