PlainRecalls

C.r. Bard Inc

117 recalls on record · Latest: May 27, 2026

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Agency notice ledger

Federal filing book C.r. Bard Inc HEAVY-BOOK · SINGLE-AGENCY

#136 of 14,151 · 117 notices · 0.112% archive

  • BOOK 117 notices
  • RANK #136 of 14,151
  • SHARE 0.112% archive
  • AGENCY FDA Devices (117)
  • CAT medical devices
  • CATS 1 category
  • LATEST May 27, 2026
  • PHOTO Snoqualmie Gourmet Ic…

Nearest notice-volume peer: Snoqualmie Gourmet Ice Cream (0 notice gap)

C.r. Bard Inc accounts for about 0.112% of the 104,423-notice archive on 117 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where C.r. Bard Inc sits among 14,151 recalling firms

C.r. Bard Inc ranks 136th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

C.r. Bard Inc vs all firms by recall-notice count

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

117 136th of 14151 higher than 14,014 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

C.r. Bard Inc in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows C.r. Bard Inc holds about 0.112% of archive notices alongside 117 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Low Aug 10, 2016

SureStep Tray, with Add-a-Foley, COMPLETE CARE, Drainage Bag, and STATLOCK Stabilization The product is a urine collection system that includes a STATLOCK Foley Stabilization Device

FDA Devices Moderate May 18, 2016

Arctic Sun Temperature Management System, 5000, 100-120V and 220-240V The product is a thermal regulating system indicated for monitoring and controlling patient temperature

FDA Devices Moderate Apr 20, 2016

BARDEX I.C. Anti-Infective 2-Way 5cc Foley Catheter. Intended for urinary bladder drainage in female patients requiring catheterization for management of incontinence, voiding dysfunction and surgical procedure.

FDA Devices Moderate Apr 20, 2016

BARDEX I.C. Anti-Infective 2-Way 3cc Foley Catheter, Rx only. Intended for urinary bladder drainage in female patients requiring catheterization for management of incontinence, voiding dysfunction and surgical procedure.

FDA Devices Moderate Apr 20, 2016

BARDEX I.C. Anti-Infective 2-Way Red Latex Foley Catheter, 5cc (Council Model); Intended for urinary bladder drainage in female patients requiring catheterization for management of incontinence, voiding dysfunction and surgical procedure.

FDA Devices Moderate Apr 20, 2016

BARD ArcticGel Pads Product Usage: The Arctic Sun Temperature Management System is intended for monitoring and controlling patient temperature. ArcticGel Pads are only for use with an Arctic Sun Temperature Management System Control Module.

FDA Devices Low Feb 24, 2016

REF 0038460 Toomey Syringe 70cc Syringe with Catheter Tip and Luer Tip Adapters, Single Use, Rx Only, Latex Free, 50 units. Product Usage: Product is intended for Resectoscope irrigation, catheter irrigation and Foley catheter inflation.

FDA Devices Moderate Feb 17, 2016

Arctic Sun 5000 and Arctic Sun 2000; Intended for monitoring and controlling patient temperatures.

FDA Devices Low Nov 11, 2015

Antibacterial Hydro Personal Catheter, Male 12 Fr, Product Code 63512, sold in boxes of 30 units

FDA Devices Moderate Sep 9, 2015

Magic3 Intermittent Catheter with Sure Grip Hydrophilic Coated Silicone Coude tip, Product Code 50614. The catheters are packaged in film-to-film pouches and packaged 30 per box. Used as an Intermittent Urinary Catheter

FDA Devices Moderate Aug 26, 2015

Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 12 Fr, (30/box), Product Code 51612. Intermittent catheter.

FDA Devices Moderate Aug 26, 2015

Magic3 Hydrophilic-coated Female Intermittent Urinary Catheter 14 Fr in the Insertion Supply Kit, Product Code 51614S. Intermittent catheter.

FDA Devices Moderate Aug 26, 2015

Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 14 Fr, (30/box), Product Code 51614. Intermittent catheter.

FDA Devices Moderate Aug 26, 2015

Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 10 Fr, (30/box), Product Code 51610. Intermittent catheter.

FDA Devices Moderate Aug 26, 2015

Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 16 Fr, (30/box), Product Code 51616. Intermittent catheter.

FDA Devices Moderate Apr 8, 2015

Bard 100% Latex-Free Urinary Drainage Bag with Anti-Reflux Chamber and Bard EX-Lok Sampling; Product Code 154006: Lot # NGYJ0603 and NGYJ1671

FDA Devices Moderate Nov 12, 2014

Bard Dimension Stone Basket Product Usage: The Bard Dimension Stone basket is a teardrop-shaped basket with the ability to capture stones by, opening and closing the basket and articulating or moving the basket from side to side. The device consists of 3 main parts; handle, shaft and basket. It is intended to use in the endoscopic removal of renal and ureteral stones.

C.r. Bard Inc carries an outsized archive share

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 (117 here — heavy-book).

Similar medical devices volume

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

Frequently Asked Questions

How many federal recall notices name C.r. Bard Inc?
PlainRecalls indexes 117 distinct federal recall events naming 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 C.r. Bard Inc sit among other recalling firms?
C.r. Bard Inc ranks #136 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of C.r. Bard Inc's notices?
FDA Devices accounts for 117 of this firm's 117 indexed notices.
What product category dominates C.r. Bard Inc's filing book?
Filings for 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.
C.r. Bard Inc: 117 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 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