C.R. Bard Inc recalls
Every recall we track for C.R. Bard Inc — 88 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from C.R. Bard Inc more than tripled in 2025 (16, up from 1 in 2024). 1% rated “stop using now”.
All FDA recall records for C.R. Bard Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 2 | 8 | 1 | 11 |
| 2018 | 0 | 4 | 0 | 0 | 4 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 2 | 0 | 2 |
| 2021 | 0 | 0 | 22 | 0 | 22 |
| 2022 | 0 | 1 | 2 | 0 | 3 |
| 2023 | 0 | 14 | 8 | 0 | 22 |
| 2024 | 0 | 0 | 1 | 0 | 1 |
| 2025 | 0 | 2 | 14 | 0 | 16 |
| 2026 (to date) | 1 | 0 | 6 | 0 | 7 |
Most common reasons for C.R. Bard Inc recalls
What to do if you have a recalled C.R. Bard Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All C.R. Bard Inc recalls
27 shown- Stop using nowMedical device
C.R. Bard Inc recalls Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿ All-Silicone Foley Catheter REF: 947314
Bard recalls certain Foley catheter trays and related products that contain Pericare wipes with contamination. Affected units include specific model numbers and UDI codes. Consumers should stop using these products to avoid potential health risks.
BardJun 25, 2026 - Lower riskMedical device
C.R. Bard Inc recalls Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley
C.R. Bard recalls Silastic Foley Catheters with a surface stain. Affected models include 30cc and 5cc sizes with specific lot numbers. No action needed as the stain is cosmetic.
C.R. BardApr 23, 2026 - Lower riskMedical device
C.R. Bard Inc recalls BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm, Ureteral Stent Kit REF 788630
C.R. Bard recalls BD InLay Optima Ureteral Stent Kit Size 6 Fr. x 30 cm (REF 788630) due to possible size mismatch with product label. Affected units may have incorrect dimensions.
C.R. BardNov 6, 2025 - Lower riskMedical device
C.R. Bard Inc recalls SureStep Foley Tray System Bardex I.C. Complete Care Infection Control Foley Catheter Tray, REF: A303316A
C.R. Bard recalls SureStep Foley Tray System with incorrect inserts that may cause infection due to material mix-ups. Affected units have REF: A303316A and Lot#NGJX6399.
C.R. BardJul 17, 2025 - Use cautionMedical device
C.R. Bard Inc recalls Bardex Lubri-Sil I.C. 400-series Temperature Sensing Silver/Hydrogel Coated All-Silicone Foley Catheter 5cc Balloon,
C.R. Bard recalls specific models of temperature-sensing silicone catheters due to potential lumen obstruction causing urinary retention and pain. Affected units include certain 5cc balloon models with specific reference numbers.
C.R. BardJun 18, 2025 - Lower riskMedical device
C.R. Bard Inc recalls REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra
C.R. Bard recalls urologist's trays with incorrect French size packaging. This may lead to improper use during procedures. Affected units include specific lot numbers.
C.R. BardJun 3, 2025 - Lower riskMedical device
C.R. Bard Inc recalls Bard¿ Single Intragastric Linton Balloon Tube, REF: 0092740
Bard recalls single intragastric linton balloon tubes with potential difficulty removing plastic plugs for inflation. Affected units have specific lot numbers and expiration dates.
BardApr 17, 2025 - Lower riskMedical device
C.R. Bard Inc recalls Bard Medical SureStep Foley Tray System, 16 Fr., Catalog #A319416AM; and Bard Medical Bardex IC Complete Care Infection
Bard Medical recalls SureStep Foley Tray Systems with potential incorrect temperature readings that could lead to infection risks. Affected units have specific lot numbers and expiration dates.
Bard MedicalMay 9, 2024 - Use cautionMedical device
C.R. Bard Inc recalls Bard¿ Nasogastric Sump Tube with ENFit, 14Fr., 48in Long, REF EN0042140
Bard recalls NG Sump Tubes with ENFit connectors due to reported inadequate suction and drainage. Affected models include specific serial numbers and sizes. Consumers should contact Bard for details.
BardDec 20, 2023 - Lower riskMedical device
C.R. Bard Inc recalls Sensica Urine Output System, Catalog Number SCCS1002
C.R. Bard recalls Sensica Urine Output System (SCCS1002) due to incorrect time displays when connected to WiFi, causing inaccurate monitoring data. Affected units have specific serial numbers listed in the recall.
C.R. BardNov 15, 2023 - Lower riskMedical device
C.R. Bard Inc recalls HydroSil Go Intermittent Urinary Catheters, Catalog Numbers: a) REF 71808, b) REF 71810, c) REF 71812, d) REF 71814, e)
C.R. Bard recalls specific HydroSil Go intermittent urinary catheters due to a potential sterility risk from a label separation defect. Affected models include catalog numbers REF 71808-71818 with listed lot numbers.
C.R. BardApr 20, 2023 - Lower riskMedical device
C.R. Bard Inc recalls Sensica Urine Output System
C.R. Bard recalls Sensica Urine Output System with catalog number SCCS1002 due to complaints about urine output measurement accuracy. Affected units include specific lot numbers listed in the recall notice.
C.R. BardMay 19, 2022 - Use cautionMedical device
C.R. Bard Inc recalls BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C
Bard recalls 14Fr SURESTEP intermittent catheter trays with potential leak at catheter-drain bag connection. Affected units have specific serial numbers. Stop using immediately to prevent leaks.
BardJan 27, 2022 - Lower riskMedical device
C.R. Bard Inc recalls Catalog A319416AM, SureStep" Foley Tray, Bardex" I.C., Complete Care", Urine Meter, Temperature Sensing, StatLock"
C.R. Bard recalls SureStep Foley Trays with potential packaging defects that could compromise sterile barrier. Affected units have specific lot numbers and expiration dates. Consumers should check their product details to determine if recalled.
BardAug 5, 2021 - Lower riskMedical device
C.R. Bard, Inc. recalls Bard Clean-Cath Intermittent Catheter, 12 French female length (catheter, urological) - Product Usage: for urological
Bard recalls 12 French female intermittent catheters due to missing tip and unsealed packaging. Affected units have specific lot numbers and expiration dates. Consumers should contact Bard for details.
BardJan 11, 2021 - Lower riskMedical device
C.R. Bard Inc recalls SureStep Foley Tray System - Product Usage: Intended for use in the drainage and/or collection and/or measurement of
C.R. Bard recalls SureStep Foley Tray System due to potential white paper residue on catheters. Affected units have specific lot numbers and expiration dates. Consumers should contact for details.
C.R. BardApr 15, 2020 - Lower riskMedical device
C.R. Bard Inc recalls The Bard Intra-abdominal Pressure Monitoring Device is composed of a tubing set used for infusing fluid into the
C.R. Bard recalls intra-abdominal pressure monitoring devices with potential for inaccurate readings due to leaks or disconnects near the sampling port. Users should confirm measurements with alternative methods.
C.R. BardJan 13, 2020 - Use cautionMedical device
C.R. Bard, Inc. recalls Bard(R) Premature Infant Feeding tube, ENFit(TM), REF EN0036430 Product Usage: BARD(R) Nasogastric Sump Tubes with
Bard recalls premature infant feeding tubes with ENFit connector due to potential poor fusion of tubing and connector. Affected units have specific lot numbers. Consumers should contact Bard for details.
BardFeb 27, 2018 - Lower riskMedical device
C.R. Bard, Inc. recalls Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter (Creevy), 22Fr. Rx (01267522)
C.R. Bard recalls specific models of Foley catheters due to incorrect retainer cap printing, which may lead to improper use. Affected units include model 01267522 with lot numbers NGBR0383 and NGB:2129.
C.R. BardDec 13, 2017 - Lower riskMedical device
C.R. Bard, Inc. recalls BARD(R) CRITICORE(R) MONITOR, Model: 000002N Series The CritiCore(R) Automated Urine Output and Temperature Monitor is
C.R. Bard recalls CritiCore monitors with serial numbers listed that may have urine output and temperature measurement fluctuations, causing potential inaccuracies in patient monitoring.
C.R. BardNov 10, 2017 - Lower riskMedical device
C.R. Bard, Inc. recalls CritiCore Automated Urine Output and Temperature Monitor
C.R. Bard recalls CritiCore Automated Urine Output and Temperature Monitors with potential urine output and temperature measurement errors and false alarms. Affected models include DYZIAA003, DYAPAA017, and other serial numbers listed in the recall.
C.R. BardNov 10, 2017 - Lower riskMedical device
C.R. Bard, Inc. recalls Medivance ArcticGel Small Pad Kit - a box containing a single foil pouch, which contains a set of four (4) pads. A set
C.R. Bard recalls ArcticGel Small Pad Kit due to hydrogel peeling from pads. This may cause skin irritation or discomfort during use. Affected units include specific product codes and lots.
C.R. BardOct 16, 2017 - Lower riskMedical device
C.R. Bard, Inc. recalls BARD UROS AUTOMATED URINE OUPTUT AND TEMPERATURE MONITOR, MODEL BK10001M The Uros(TM) Automated Urine Output and
C.R. Bard recalls Uros Automated Urine Output and Temperature Monitor (BK10001M) due to potential inaccurate urine measurements affecting clinical decisions. Affected users should contact for details.
C.R. BardSep 29, 2017 - UnratedMedical device
C.R. Bard, Inc. recalls HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual
C.R. Bard recalls 10" HydroSil Gripper intermittent catheters (30 per box) due to potential catheter cutting during use. Affected lots include JUBT0404, JUBP0700, JUBR2498, JUBS1289. No remedy specified in recall notice.
C.R. BardSep 14, 2017 - Lower riskMedical device
C.R. Bard, Inc. recalls Bard Magic 3 Antibacterial Hydrophilic Intermittent Catheter Female, 14 FR (30/box), Rx Only intended for urinary
C.R. Bard recalls specific lots of Magic 3 Antibacterial Hydrophilic Intermittent Catheters that may lack the hydrophilic coating, increasing infection risk. Affected units have catalog numbers 51514 and lots 53623024, 53623054, 53623047, 53623122.
C.R. BardJul 28, 2017 - Lower riskMedical device
C.R. Bard, Inc. recalls Arctic Sun ArcticGel Pads - Medium, Product Code 317-07
C.R. Bard recalls Arctic Sun ArcticGel Pads (Product Code 317-07) due to incorrect box labeling. This may cause confusion but does not pose a safety risk.
C.R. BardJun 2, 2017 - Lower riskMedical device
C.R. Bard, Inc. recalls BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension, Extension Tube and Latex Straps, 19 oz. Packaged as
C.R. Bard recalls leg bags with flip-flo valve that may have cuts in the sterile barrier, risking infection. Check product code 151919 for affected units.
C.R. BardJun 2, 2017
C.R. Bard Inc recall questions
How many recalls has C.R. Bard Inc had?
88 recalls from C.R. Bard Inc are on record with U.S. safety agencies, from 2017–2026.
What is the most recent C.R. Bard Inc recall?
C.R. Bard Inc recalls Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿ All-Silicone Foley Catheter REF: 947314, dated Jun 25, 2026. Every C.R. Bard Inc recall is listed on this page, newest first.
Why are C.R. Bard Inc products recalled?
The most common reasons on record: There is potential for packaging defects that may impact the sterile barrier. (21); Cather packaging may contain the incorrect French size. (3).
What should I do if I have a recalled C.R. Bard Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new C.R. Bard Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.