The Recall Desk

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.

1–25 of 123

  • HighFDA (Devices)·Z-3118-2026·2026-09-16

    C.R. Bard Recalls SureStep Foley Trays Due to Wipe Contamination

    C.R. Bard is recalling SureStep Foley and Intermittent Catheter Trays because complaints indicated contamination on the surface of the included Pericare wipes.

    Product
    Products that contain the Pericare Wipes: SureStep" Foley Tray System Add-A-Foley Catheter REF: A153200 UDI code: 00801741121067¿ 10801741121064 SureStep" Foley Tray System Complete Care¿ Add-A-Foley Catheter REF: A304400A UDI code: 00801741073847¿ 10801741073844 SureStep"…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3117-2026·2026-09-16

    C.R. Bard Recalls SureStep Catheter Trays Due to Wipe Contamination

    C.R. Bard is recalling SureStep Intermittent Catheter Trays because complaints indicated contamination on the surface of the included Pericare wipes.

    Product
    Products that contain the Pericare Wipes: SureStep Intermittent Catheter Tray REF: INTP16 INTS14 INTS14C INTS16 INTS16C PEDINTS06 PEDINTS08 PEDINTS10 UDI code: 00801741183300¿ 10801741183307 00801741183218¿ 10801741183215 00801741183232 10801741183239 00801741183225¿…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3114-2026·2026-09-16

    C.R. Bard Recalls Foley Catheter Trays Due to Wipe Contamination

    C.R. Bard is recalling 12,463 Foley and intermittent catheter trays because complaints indicated contamination on the surface of the included Pericare wipes.

    Product
    Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes: 00801741024801¿ 10801741024808 00801741024818¿ 10801741024815 00801741024825¿ 10801741024822 SureStep" Foley Tray System with Bardex¿ Lubricath Temp…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3119-2026·2026-09-16

    C.R. Bard Recalls SureStep Foley Trays Due to Wipe Contamination

    C.R. Bard Inc. is recalling SureStep Foley and Intermittent Catheter Trays because complaints indicated contamination on the surface of the included Pericare wipes.

    Product
    Products that contain the Pericare Wipes: (Canada Only) SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A300314AC UDI-DI code: 00801741143243 SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A300316AC UDI-DI code: 00801741143250 SureStep" Foley Tray…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3116-2026·2026-09-16

    C.R. Bard Recalls Foley Catheter Trays Due to Wipe Contamination

    C.R. Bard Inc. is recalling specific Bardex and SureStep Foley catheter trays because complaints indicated surface contamination on the included Pericare wipes.

    Product
    Products that contain the Pericare Wipes: *Bardex¿ I.C. Complete Care¿ Foley Catheter Tray REF: 300316A UDI codes: 00801741024344¿ 10801741024341 *Bardex¿ I.C. Complete Care¿ Foley Catheter Tray and Urine Meter REF: 303314A 303316A 303318A UDI code: 00801741024252¿…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3115-2026·2026-09-16

    C.R. Bard Recalls Foley Catheter Trays Due to Wipe Contamination

    C.R. Bard Inc is recalling specific Foley and Intermittent Catheter Trays because complaints indicated contamination on the surface of the included Pericare wipes.

    Product
    Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿ All-Silicone Foley Catheter REF: 947314 947316 947318 UDI codes: 00801741024924¿ 10801741024921 00801741024931¿ 10801741024938 00801741024948¿ 10801741024945 Lubri-Sil¿ I.C. Complete Care¿ All-Silicone…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2226-2026·2026-05-27

    Silastic Brand Foley Catheters recalled due to surface stain

    C.R. Bard Inc is recalling Silastic Brand Foley Catheters because of stain present on the surface of affected units. The recall affects 106,160 catheters distributed across the United States and Canada.

    Product
    Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley Catheter 5cc REF: 33614 33616 33618 33620 33622 33624
    Category
    Medical Device
    Distribution
    44 states
  • ModerateFDA (Devices)·Z-0907-2026·2025-12-17

    Ureteral stent kits recalled because the stent size may not match the label

    C.R. Bard is recalling 116 BD InLay Optima Ureteral Stent Kits, 6 Fr x 30 cm, because the actual stent size may not match the product label.

    Product
    BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm, Ureteral Stent Kit REF 788630
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0908-2026·2025-12-17

    Ureteral stent kits, 8 French, recalled over a size labeling discrepancy

    C.R. Bard is recalling 116 BD InLay Optima Ureteral Stent Kits, 8 Fr x 26 cm, because the actual stent size may not match the product label.

    Product
    BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm, Ureteral Stent Kit REF 78826
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0905-2026·2025-12-17

    Short ureteral stent kits recalled over a size labeling discrepancy

    C.R. Bard is recalling 116 Bard InLay Optima Ureteral Stent Kits, 6 Fr x 14 cm, because the actual stent size may not match the product label.

    Product
    Bard InLay Optima Size: 6 Fr. x 14 cm, Ureteral Stent Kit REF 787614
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0906-2026·2025-12-17

    Ureteral stent kits, 4.7 French, recalled over a size labeling discrepancy

    C.R. Bard is recalling 4,350 BD InLay Optima Ureteral Stent Kits, 4.7 Fr x 26 cm, because the actual stent size may not match the product label.

    Product
    BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm, Ureteral Stent Kit REF 788426
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2589-2025·2025-09-24

    Bardex Foley catheter trays recalled over inserts describing the wrong material

    SureStep Foley Tray Systems, REF A303316A lot NGJX6399, are recalled because incorrect inserts may lead users to misidentify the catheter material or coating, risking infection or allergic reaction.

    Product
    SureStep Foley Tray System Bardex I.C. Complete Care Infection Control Foley Catheter Tray, REF: A303316A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2591-2025·2025-09-24

    Lubri-Sil Foley trays recalled over inserts describing the wrong catheter material

    SureStep Foley Tray Systems with Bard Lubri-Sil catheters, REF A942216 lot NGJX4320, are recalled because incorrect inserts may lead users to misidentify the catheter material or coating. 3,670 units are affected.

    Product
    SureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray, REF: A942216
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2590-2025·2025-09-24

    Foley catheter trays recalled because inserts describe the wrong catheter material

    SureStep Foley Tray Systems, REF A303414A lot NGJY3685, are recalled because incorrect inserts may lead users to misidentify the catheter material or coating, risking infection or allergic reaction.

    Product
    SureStep Foley Tray System Lubri-Sil I.C. Complete Care Infection Control Foley Catheter Tray, REF: A303414A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2462-2025·2025-09-03

    Foley catheters recalled because obstructed lumen may prevent bladder drainage

    Bardex Lubri-Sil I.C. Foley catheters and related tray systems are recalled because the catheter may have an obstructed lumen, which may prevent the bladder from draining. 175,158 units are affected.

    Product
    Bardex Lubri-Sil I.C. 400-series Temperature Sensing Silver/Hydrogel Coated All-Silicone Foley Catheter 5cc Balloon, REF: 119314; SureStep Foley Tray System Lubri-Sil I.C. Complete Care, REF: A319514A; Bard Silver Lubri-Sil Foley Tray Temperature Sensing with Bard Hydrogel…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2076-2025·2025-07-09

    Bard Urologist's Tray Recalled Over Incorrect French Size Labeling

    C.R. Bard Inc is recalling 63 units of the Bard Urologist's Tray due to cather packaging that may contain the incorrect French size, which could affect device use.

    Product
    REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2074-2025·2025-07-09

    BD Heyman Follower Straight Tip catheters with incorrect French size packaging

    C.R. Bard Inc is recalling BD Heyman Follower Straight Tip catheters because packaging may contain an incorrect French size designation, which could lead to use of the wrong catheter size.

    Product
    BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr - REF:21112, 14Fr - REF: 21114, 20Fr - REF: 21120
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2075-2025·2025-07-09

    BD Heyman Coude Tip Catheters Recalled Over French Size Labeling Error

    C.R. Bard Inc is recalling certain BD Heyman Follower Coude Tip catheters because the packaging may display the incorrect French size, which could lead to use of the wrong size device.

    Product
    BD Heyman Follower Coude Tip for following sizes: 12Fr - REF:021312 14Fr - REF:021314, 16Fr - REF: 021316
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1757-2025·2025-05-28

    Bard Blakemore Esophageal-Nasogastric Tube Child Difficult Plug Removal

    C.R. Bard is recalling Bard Blakemore Esophageal-Nasogastric Tubes (Child) due to customer complaints that plastic plugs may be difficult or impossible to remove, preventing inflation of the gastric and esophageal balloons.

    Product
    Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) REF: 0092110
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Devices)·Z-1758-2025·2025-05-28

    Bard Blakemore Esophageal-Nasogastric Tube Intermediate Balloon Inflation Difficulty

    C.R. Bard Inc is recalling Bard Blakemore Esophageal-Nasogastric Tubes (Intermediate, REF 0092300) due to reports that plastic plugs may be difficult or impossible to remove, preventing proper inflation of the gastric and/or esophageal balloons.

    Product
    Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate)REF: 0092300
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Devices)·Z-1759-2025·2025-05-28

    Bard Single Intragastric Linton Balloon Tube difficult plastic plug removal

    C.R. Bard Inc is recalling the Bard Single Intragastric Linton Balloon Tube (REF: 0092740) because users may be unable or find it difficult to remove plastic plugs needed to inflate the gastric and esophageal balloons.

    Product
    Bard¿ Single Intragastric Linton Balloon Tube, REF: 0092740
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Devices)·Z-1756-2025·2025-05-28

    Bard Blakemore Esophageal-Nasogastric Tube difficult balloon inflation

    C.R. Bard is recalling Bard Blakemore Esophageal-Nasogastric Tubes (Adult) because users may find it difficult or impossible to remove the plastic plugs needed to inflate the gastric and esophageal balloons.

    Product
    Bard Blakemore Esophageal-Nasogastric Tube (Adult) REF: 0092100
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Devices)·Z-1755-2025·2025-05-28

    Bard Minnesota Four Lumen Esophagogastric Tamponade Tube Recalled

    C.R. Bard Inc is recalling the Bard Minnesota Four Lumen Esophagogastric Tamponade Tube (REF:0092220) because users may be unable to or have difficulty removing plastic plugs needed to inflate the gastric and esophageal balloons.

    Product
    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 Rubber
    Category
    Medical Device
    Distribution
    52 states
  • HighFDA (Devices)·Z-2154-2024·2024-06-26

    Bard Foley Catheter Trays Recalled for Temperature Display Malfunction

    C.R. Bard Inc is recalling 6,420 Foley catheter trays nationwide because some devices may not display temperature readings or may display erratic readings. The malfunction could affect patient monitoring.

    Product
    Bard Medical SureStep Foley Tray System, 16 Fr., Catalog #A319416AM; and Bard Medical Bardex IC Complete Care Infection Control Temperature-Sensing Foley Catheter Tray with Bard Hydrogel and Bacti-Guard Silver Alloy Coating, 350 ml Urine Meter, 16 Fr, Catalog #319416AM. Intended…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0794-2024·2024-01-31

    Bard Nasogastric Sump Tubes recalled due to inadequate suction and drainage

    C.R. Bard is recalling 37,059 units of Bard Nasogastric Sump Tubes with ENFit due to user reports of inadequate suction, decompression, and drainage during use.

    Product
    Bard¿ Nasogastric Sump Tube with ENFit, 18Fr., 48in Long, REF EN0042180
    Category
    Medical Device
    Distribution
    0 states