Manufacturer

C.R. Bard, Inc.

123 recalls in our database name C.R. Bard, Inc. as the manufacturing or recalling firm.

What the numbers show

Total: 123
Critical: 0
Severe: 6
Most recent: 2026-09-16

Of the 123 recalls from C.R. Bard, Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 6 (5%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

76–100 of 123

HighFDA (Devices)·Z-1356-2018·2018-04-18
Bard Feeding Tubes Recalled for Ineffective Connector Fusion
C.R. Bard is recalling specific lots of Bard Adult/Pediatric Feeding Tubes because the tubing and ENFit connector may not be fused effectively.
Product
Bard(R) Adult/Pediatric Feeding Tube, ENFit(TM), REF EN0036420 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1355-2018·2018-04-18
Bard Infant Feeding Tube Recalled for Ineffective Connector Fusion
C.R. Bard is recalling 23,400 infant feeding tubes because the tubing and connector may not be effectively fused.
Product
Bard(R) Infant Feeding Tube, ENFit(TM), REF EN0036410 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term tube…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1357-2018·2018-04-18
Bard Premature Infant Feeding Tubes Recalled for Ineffective Fusion
C.R. Bard is recalling specific lots of Bard Premature Infant Feeding Tubes because the tubing and ENFit connector may not be effectively fused.
Product
Bard(R) Premature Infant Feeding tube, ENFit(TM), REF EN0036430 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1354-2018·2018-04-18
Bard Premature Infant Feeding Tube Recalled for Ineffective Fusion
C.R. Bard is recalling 42,200 units of Bard Premature Infant Feeding Tubes due to potentially ineffective fusion between the tubing and the ENFit connector.
Product
Bard(R) Premature Infant Feeding Tube, ENFit(TM), REF EN0036400 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1307-2018·2018-04-11
C.R. Bard Recalls HydroSil Gripper Intermittent Catheters Due to Seal Defects
C.R. Bard is recalling specific lots of HydroSil Gripper Intermittent Catheters because some units were found caught in the sterile barrier seal or cut.
Product
HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual pouch. MGC3 Product Usage Intermittent catheters are intended for urinary bladder drainage in patients requiring catheterization for management of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1308-2018·2018-04-11
C.R. Bard Recalls Magic 3 Intermittent Catheters Due to Seal Defects
C.R. Bard is recalling Magic 3 Intermittent Catheters because some units were caught in the sterile barrier seal or cut.
Product
Magic 3 Intermittent Catheters- 12 Male - 30 catheters per box, each catheter is packaged in an individual pouch. Urinary catheter.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1309-2018·2018-04-11
C.R. Bard Recalls Personal Intermittent Catheters Due to Seal Defects
C.R. Bard is recalling Personal Intermittent Catheters because some units were found caught in the sterile barrier seal or cut.
Product
Personal Intermittent Catheters- 16" and 10" lengths - 30 catheters per box, each catheter is packaged in an individual pouch, Item Numbers: 50612, 50614, 50616, 50618, 52306, 52308, 52310, 52606, 52606G, 52608, 52608G, 52610, 52610G, 53314, 53320, 53514G, 53610, 53610G…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0565-2018·2018-02-21
C.R. Bard Recalls CritiCore Monitors Due to Measurement and Alarm Failures
C.R. Bard is recalling 343 CritiCore monitors because they may experience urine output and temperature measurement fluctuations and alarm errors.
Product
BARD(R) CRITICORE(R) MONITOR, Model: 000002N Series The CritiCore(R) Automated Urine Output and Temperature Monitor is indicated to monitor urine output and core bladder temperature.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0488-2018·2018-02-07
C.R. Bard Recalls Uros Automated Urine Output and Temperature Monitor
C.R. Bard is recalling two units of the Uros Automated Urine Output and Temperature Monitor in Florida due to potential measurement inaccuracies.
Product
BARD UROS AUTOMATED URINE OUPTUT AND TEMPERATURE MONITOR, MODEL BK10001M The Uros(TM) Automated Urine Output and Temperature Monitor is indicated to monitor urine output and core bladder temperature.
Category
Medical Device
Distribution
1 state
ModerateFDA (Devices)·Z-0271-2018·2017-12-27
C.R. Bard Recalls Medivance ArcticGel Small Pad Kits Due to Peeling
C.R. Bard is recalling 24 Medivance ArcticGel Small Pad Kits because the hydrogel is peeling from the pads. The affected units were distributed to 10 US states.
Product
Medivance ArcticGel Small Pad Kit - a box containing a single foil pouch, which contains a set of four (4) pads. A set of pads comprise a left and a right torso pad, and a left and a right thigh pad. Is a Thermal regulating system, indicated for monitoring and controlling…
Category
Medical Device
Distribution
10 states
ModerateFDA (Devices)·Z-0267-2018·2017-12-27
C.R. Bard Recalls I-125 QuickLink Cartridges Due to Incorrect Quantity
C.R. Bard is recalling I-125 QuickLink Cartridges because the quantity of seeds sent in shipments was incorrect.
Product
I-125 CE Marked QuickLink Cartridges; Sterile; Bard Brachysource Radioactive Seeds in QuickLink Cartridges Indicated for permanent interstitial treatment of selected localized tumors such as: head and neck, lung, pancreas, and early stage prostate. Implants are indicated to…
Category
Medical Device
Distribution
0 states
LowFDA (Devices)·Z-0590-2018·2017-12-13
C.R. Bard Recalls Arctic Sun ArcticGel Pads Due to Labeling Error
C.R. Bard is recalling 128 units of Arctic Sun ArcticGel Pads - Medium because the product box displays an incorrect reference number.
Product
Arctic Sun ArcticGel Pads - Medium, Product Code 317-07
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-3226-2017·2017-10-04
Bard Magic 3 Antibacterial Catheters Recalled for Missing Coating
C.R. Bard is recalling specific lots of Bard Magic 3 Antibacterial Hydrophilic Intermittent Catheters because they may lack the hydrophilic coating.
Product
Bard Magic 3 Antibacterial Hydrophilic Intermittent Catheter Female, 14 FR (30/box), Rx Only intended for urinary bladder drainage in patients requiring catheterization for management of incontinence, voiding dysfunction, and surgical procedures.
Category
Medical Device
Distribution
23 states
HighFDA (Devices)·Z-3042-2017·2017-08-23
C.R. Bard Recalls Arctic Sun 5000 Temperature Management Systems
C.R. Bard is recalling 3,450 Arctic Sun 5000 Temperature Management Systems due to potential failure if used for more than 2,000 hours without preventive maintenance.
Product
Arctic Sun 5000 Temperature Management System, 100-120 V North America and 100-120 V US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2872-2017·2017-08-16
C.R. Bard Recalls Leg Bags Due to Potential Sterile Barrier Breach
C.R. Bard is recalling 2,350 units of Bard Dispoz-A-Bag leg bags due to a reported cut in the side that may compromise the sterile barrier.
Product
BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension, Extension Tube and Latex Straps, 19 oz. Packaged as single unit in thermoformed trays. There are 50 units per case. Product Usage: Vinyl leg bag to be used with male external catheters, Foley catheters, or…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1871-2017·2017-04-26
C.R. Bard Recalls SURESTEP Drainage Bags Due to Latex Mislabeling
C.R. Bard is recalling 5,030 SURESTEP Drainage Bags because they are labeled as latex-free but may contain natural rubber latex.
Product
SURESTEP Tray, Bardex I.C. Complete Care Drainage Bag, 2000 ml Drainage Bag, 16 Fr., Sterile.
Category
Medical Device
Distribution
24 states
HighFDA (Devices)·Z-0967-2017·2017-01-18
C.R. Bard Recalls Medical Devices Containing Latex Catheters
C.R. Bard is recalling specific medical device trays and stabilization devices because they contained latex catheters instead of silicone catheters.
Product
SURESTEP Tray, BARDEX I.C. COMPLETE CARE, Urine Meter, Temperature STATLOCK Stabilization Device
Category
Medical Device
Distribution
23 states
ModerateFDA (Devices)·Z-0735-2017·2016-12-21
C.R. Bard Recalls 70cc Irrigation Syringes Due to Package Defect
C.R. Bard is recalling 452,728 units of 70cc irrigation syringes because a package defect may compromise product sterility.
Product
BARD¿ Irrigation, Syringe 70cc With Resectoscope Tip, Catheter Tip, Luer Adapter And Cap, Rx Only, Sterile, The BARD¿ Syringe is available in a single use plastic design which features a 60cc or 70cc capacity graduated barrel. It has a thumb ring plunger for one-handed use. A…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0736-2017·2016-12-21
C.R. Bard Recalls 70cc Piston Syringes Due to Package Defect
C.R. Bard is recalling 70cc Piston Syringes because a package slit defect may compromise product sterility.
Product
BARD¿ 70cc Piston Syringe with Catheter Tip, Luer Adapter and Cap, Rx Only, The BARD¿ Syringe is available in a single use plastic design which features a 60cc or 70cc capacity graduated barrel. It has a thumb ring plunger for one-handed use. A catheter adapter tip and Luer…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0737-2017·2016-12-21
C.R. Bard Recalls Piston Syringes Due to Package Defect Risk
C.R. Bard is recalling specific lots of 60cc Piston Syringes because a package slit defect may compromise product sterility.
Product
BARD¿ Piston Syringe, 60cc, Rx Only, Sterile, The BARD¿ Syringe is available in a single use plastic design which features a 60cc or 70cc capacity graduated barrel. It has a thumb ring plunger for one-handed use. A catheter adapter tip and Luer adapter tip are included. BARD¿…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0738-2017·2016-12-21
C.R. Bard Recalls BARDIA 60cc Piston Irrigation Syringes Due to Package Defect
C.R. Bard is recalling BARDIA 60cc Piston Irrigation Syringes because a slit defect in the packaging may compromise product sterility.
Product
BARDIA¿ 60cc Piston Irrigation Syringe, Sterile, Rx Only, The BARD¿ Syringe is available in a single use plastic design which features a 60cc or 70cc capacity graduated barrel. It has a thumb ring plunger for one-handed use. A catheter adapter tip and Luer adapter tip are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0585-2017·2016-11-23
C.R. Bard Recalls C-Max Cutting Loop Electrodes Due to Defect
C.R. Bard is recalling 70 units of C-Max Cutting Loop Electrodes because the contact part could separate, affecting device functionality.
Product
C-Max" Cutting Loop Electrodes, Storz One-Stem, 24 Fr, .014in., .35 mm, Sterile, Rx only, Manufactured by: C.R. Bard, Inc., Covington, GA 30014.
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-0405-2017·2016-11-23
Bard Inlay Optima Ureteral Stent Recalled for Labeling Update
C.R. Bard is recalling 75,089 Bard Inlay Optima ureteral stents to add a warning about potential knots during removal.
Product
Bard Inlay Optima¿ Multi-Length Ureteral Stent Coated Double Pigtail Ureteral Stent with Stent and Multi- Length Ureteral Stent with Suture, Manufacturer: C.R. Bard, Inc., Covington, GA 30014.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0406-2017·2016-11-23
C.R. Bard Recalls Totalis Endo Kits for Labeling Update
C.R. Bard is recalling 75,089 Totalis endo kits to add a warning about potential knots during removal.
Product
Totalis, RIGID and Totalis"I Flex ENDO KIT, Manufacturer: C.R. Bard, Inc., Covington, GA 30014.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0403-2017·2016-11-23
Bard Fluoro-4 Silicone Ureteral Stent Recall for Labeling Update
C.R. Bard is recalling 75,089 units of Bard Fluoro-4 Silicone Ureteral Stents to add a warning about potential knots during removal.
Product
Bard Fluoro-4 Silicone Ureteral Stent, Bard¿ Fluoro-4", Silicone Ureteral Coil Stent; Bard¿ Silicone Uretera l Coil Stent with Figure Four, End, Manufacturer: C.R. Bard, Inc., Covington, GA 30014.
Category
Medical Device
Distribution
Distributed nationwide