PlainRecalls

C.r. Bard, Inc.

Compiled from official public sources by the editorial team.

117 recalls on record · Latest: May 27, 2026

C.r. Bard, Inc. Recall Insight

C.r. Bard, Inc. appears on 117 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.115% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated May 27, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 5 critical, 45 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 48 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Sep 29, 2021 to May 27, 2026.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate May 27, 2026

Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley Catheter 5cc REF: 336…

FDA Devices Moderate Dec 17, 2025

BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm, Ureteral Stent Kit REF 788630

FDA Devices Moderate Dec 17, 2025

Bard InLay Optima Size: 6 Fr. x 14 cm, Ureteral Stent Kit REF 787614

FDA Devices Moderate Dec 17, 2025

BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm, Ureteral Stent Kit REF 788426

FDA Devices Moderate Dec 17, 2025

BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm, Ureteral Stent Kit REF 78826

FDA Devices Moderate Sep 24, 2025

SureStep Foley Tray System Bardex I.C. Complete Care Infection Control Foley Catheter Tray, REF: A303316A

FDA Devices Moderate Sep 24, 2025

SureStep Foley Tray System Lubri-Sil I.C. Complete Care Infection Control Foley Catheter Tray, REF: A303414A

FDA Devices Moderate Sep 24, 2025

SureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray, REF: A942216

FDA Devices Moderate Sep 3, 2025

Bardex Lubri-Sil I.C. 400-series Temperature Sensing Silver/Hydrogel Coated All-Silicone Foley Catheter 5cc Balloon, REF: 119314; SureStep Foley Tr…

FDA Devices Moderate Jul 9, 2025

REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra

FDA Devices Moderate Jul 9, 2025

BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr - REF:21112, 14Fr - REF: 21114, 20Fr - REF: 21120

FDA Devices Moderate Jul 9, 2025

BD Heyman Follower Coude Tip for following sizes: 12Fr - REF:021312 14Fr - REF:021314, 16Fr - REF: 021316

FDA Devices Critical May 28, 2025

Bard¿ Single Intragastric Linton Balloon Tube, REF: 0092740

FDA Devices Critical May 28, 2025

Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate)REF: 0092300

FDA Devices Critical May 28, 2025

Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) REF: 0092110

FDA Devices Critical May 28, 2025

Bard Minnesota Four Lumen Esophagogastric Tamponade Tube, REF:0092220 18 Fr. (6mm, 7/32"), 41" Length (104cm) with 8" (20.3cm) Balloon X-Ray Opaque R…

FDA Devices Critical May 28, 2025

Bard Blakemore Esophageal-Nasogastric Tube (Adult) REF: 0092100

FDA Devices Moderate Jun 26, 2024

Bard Medical SureStep Foley Tray System, 16 Fr., Catalog #A319416AM; and Bard Medical Bardex IC Complete Care Infection Control Temperature-Sensing F…

FDA Devices Moderate Jan 31, 2024

Bard¿ Nasogastric Sump Tube with ENFit, 14Fr., 48in Long, REF EN0042140

FDA Devices Moderate Jan 31, 2024

Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 18Fr., 48in Long, REF EN0046180

FDA Devices Moderate Jan 31, 2024

Bard¿ Nasogastric Sump Tube with ENFit, 18Fr., 48in Long, REF EN0042180

FDA Devices Moderate Jan 31, 2024

Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 14Fr., 48in Long, REF EN0046140

FDA Devices Moderate Jan 31, 2024

Bard¿ Nasogastric Sump Tube and PreVent¿ Filter and Lopez Valve¿ with ENFit, 14Fr., 48in Long, REF EN0056140

FDA Devices Moderate Jan 31, 2024

Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit", 12Fr., 48in Long, REF EN0046120

FDA Devices Moderate Jan 31, 2024

Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 10Fr., 36in Long, REF EN0046100

FDA Devices Moderate Jan 31, 2024

Bard¿ Lopez Valve¿ with ENFit, REF EN0056000

FDA Devices Moderate Jan 31, 2024

Bard¿ Nasogastric Sump Tube and PreVent¿ Anti-Reflux Filter and Lopez Valve¿ with ENFit, 18Fr., 48in Long, REF EN0056180

FDA Devices Moderate Jan 31, 2024

Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 16Fr., 48in Long, REF EN0046160

FDA Devices Moderate Jan 31, 2024

Bard¿ PreVent¿ Anti-Reflux Filter with ENFit, REF EN0046000

FDA Devices Moderate Jan 31, 2024

Bard Nasogastric Sump Tube with ENFit, 10Fr., 36in Long, REF EN0042100

FDA Devices Moderate Jan 31, 2024

Bard¿ Suction Connector with ENFit, REF EN0066000

FDA Devices Moderate Jan 31, 2024

Bard¿ Nasogastric Sump Tube and PreVent¿ Anti-Reflux Filter and Lopez Valve¿ with ENFit, 12Fr., 48in Long, REF EN0056120

FDA Devices Moderate Jan 31, 2024

Bard¿ Nasogastric Sump Tube and PreVent¿ Filter and Lopez Valve¿ with ENFit, 16Fr., 48in Long , REF EN0056160

FDA Devices Moderate Jan 31, 2024

Bard¿ Nasogastric Sump Tube with ENFit, 16Fr., 48in Long, REF EN0042160

FDA Devices Moderate Jan 31, 2024

Bard¿ Nasogastric Sump Tube with ENFit, 12Fr., 48in Long, REF EN0042120

FDA Devices Moderate Dec 20, 2023

Sensica Urine Output System, Catalog Number SCCS1002

FDA Devices Moderate Jun 14, 2023

HydroSil Go Intermittent Urinary Catheters, Catalog Numbers: a) REF 71808, b) REF 71810, c) REF 71812, d) REF 71814, e) REF 71816, f) REF 71818

FDA Devices Moderate Jun 14, 2023

Magic3 Go Intermittent Urinary Catheters, Female Catalog Numbers: a) REF 51808, b) REF 51810, c) REF 51812, d) REF 51814, e) REF 51816, f) REF 51818

FDA Devices Moderate Jun 14, 2023

Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G

FDA Devices Moderate Jun 14, 2023

Magic3 Go Intermittent Urinary Catheters, male Catalog Numbers: a) REF 50810G, b) REF 50812G, c) REF 50814G, d) REF 50816G, e) REF 50818G, f) REF 538…

FDA Devices Moderate Jul 6, 2022

Sensica Urine Output System

FDA Devices Moderate Mar 2, 2022

BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C

FDA Devices Moderate Mar 2, 2022

BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS16C

FDA Devices Moderate Sep 29, 2021

Catalog A319416AM, SureStep" Foley Tray, Bardex" I.C., Complete Care", Urine Meter, Temperature Sensing, StatLock" Stabilization Device

FDA Devices Moderate Sep 29, 2021

Catalog A800360, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray

FDA Devices Moderate Sep 29, 2021

Catalog A899916, SureStep" Foley Tray, Lubricath", Drainage Bag, StatLock" Stabilization Device

FDA Devices Moderate Sep 29, 2021

Catalog A942216, SureStep" Foley Tray, Bard LubricathTM, Urine Meter, StatLock" Stabilization Device

FDA Devices Moderate Sep 29, 2021

Catalog A897514, SureStep" Foley Tray, Silicone, Drainage Bag, StatLock" Stabilization Device

FDA Devices Moderate Sep 29, 2021

Catalog A902616, SureStep" Foley Tray, Bardex" I.C., Lubricath", Urine Meter

FDA Devices Moderate Sep 29, 2021

Catalog A800061, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare C.r. Bard, Inc. with Zimmer Biomet, Inc. →

Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.