PlainRecalls

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

20 recalls on record · Latest: Nov 19, 2014

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Agency notice ledger

Federal filing book Davol, Inc., Subs. C. R. Ba… MID-BOOK · SINGLE-AGENCY

#800 of 14,151 · 20 notices · 0.019% archive

  • BOOK 20 notices
  • RANK #800 of 14,151
  • SHARE 0.019% archive
  • AGENCY FDA Devices (20)
  • CAT medical devices
  • CATS 1 category
  • LATEST Nov 19, 2014
  • PHOTO AbbVie Inc.

Nearest notice-volume peer: AbbVie Inc. (0 notice gap)

Davol, Inc., Subs. C. R. Bard, Inc. accounts for about 0.019% of the 104,423-notice archive on 20 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Davol, Inc., Subs. C. R. Ba…'s standing among 14,151 recalling firms

Davol, Inc., Subs. C. R. Bard, Inc. ranks 800th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Davol, Inc., Subs. C. R. Ba… vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

20 800th of 14151 higher than 13,326 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Davol, Inc., Subs. C. R. Ba… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Davol, Inc., Subs. C. R. Bard, Inc. holds about 0.019% of archive notices alongside 20 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Nov 19, 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.

FDA Devices Moderate Jun 11, 2014

Composix" LP with Echo PS" 6x10 Reorder Number: 0144610 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Devices Moderate Jun 11, 2014

Bard¿ Ventralight" ST Mesh with Echo PS" 8"x10" Reorder Number: 5955810 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Devices Moderate Jun 11, 2014

Bard¿ Ventralight" ST Mesh with Echo PS" 12"x14" Reorder Number: 5955124 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Devices Moderate Jun 11, 2014

Bard¿ Composix" LIP Mesh with Echo PS" 7"x9" Reorder Number: 0144790 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Devices Moderate Jun 11, 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.

FDA Devices Moderate Jun 11, 2014

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.

FDA Devices Moderate Jun 11, 2014

Composix" LP with Echo PS" 6x8 Reorder Number: 0144680 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Devices Moderate Jun 11, 2014

Bard¿ Ventralight" ST Mesh with Echo PS" 4"x6" Reorder Number: 5955460 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Devices Moderate Jun 11, 2014

Bard¿ Ventralight" ST Mesh with Echo PS" 6"x10" Reorder Number: 5955610 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Devices Moderate Jun 11, 2014

Bard¿ Composix" LIP Mesh with Echo PS" 8"x10" Reorder Number: 0144810 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Devices Moderate Jun 11, 2014

Bard¿ Ventralight" ST Mesh with Echo PS" 6"x8" Reorder Number: 5955680 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Devices Moderate Jun 11, 2014

Bard¿ Ventralight" ST Mesh with Echo PS" 6" CircleReorder Number: 5955600 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Devices Moderate Jun 11, 2014

Bard¿ Ventralight" ST Mesh with Echo PS" 8" Circle Number: 5955800 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Devices Moderate Jun 11, 2014

Bard¿ Ventralight" ST Mesh with Echo PS" 4.5" Circle Reorder Number: 5955450 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Devices Moderate Jun 11, 2014

Bard¿ Ventralight" ST Mesh with Echo PS TM 7"x9" Reorder Number: 5955790 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Devices Moderate Jan 29, 2014

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-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 laproscopic ventral hernia repair.

FDA Devices Moderate 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 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 laproscopic ventral hernia repair.

FDA Devices Moderate 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 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 deficiencies, such as for the repair of hernias.

FDA Devices Moderate Sep 26, 2012

Bard Ventralight ST Mesh. - Ellipse 7" x 9" (17.8 cm x 22.9 cm) Product Code 5954790. 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 deficiencies, such as for the repair of hernias.

Davol, Inc., Subs. C. R. Ba… holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (20 here).

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Frequently Asked Questions

How many federal recall notices name Davol, Inc., Subs. C. R. Ba…?
PlainRecalls indexes 20 distinct federal recall events naming Davol, Inc., Subs. C. R. Bard, Inc., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Davol, Inc., Subs. C. R. Ba… sit among other recalling firms?
Davol, Inc., Subs. C. R. Bard, Inc. ranks #800 of 14,151 by distinct recall-event count among 14,151 firms in this archive (94th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Davol, Inc., Subs. C. R. Ba…'s notices?
FDA Devices accounts for 20 of this firm's 20 indexed notices.
What product category dominates Davol, Inc., Subs. C. R. Ba…'s filing book?
Filings for Davol, Inc., Subs. C. R. Bard, Inc. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous?
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Davol, Inc., Subs. C. R. Bard, Inc.: 20 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Davol, Inc., Subs. C. R. Bard, Inc.; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026