C.R. Bard Recalls
117 recalls on record · November 12, 2014 to May 27, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 27, 2026Medical DevicesFDA
C.R. Bard Inc recalls Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand
Hazard: Due to stain present on the surface of affected foley catheters.
December 17, 2025Medical DevicesFDA
C.R. Bard Inc recalls BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm, Ureteral Stent Kit REF 78826
Hazard: Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
December 17, 2025Medical DevicesFDA
C.R. Bard Inc recalls BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm, Ureteral Stent Kit REF 788630
Hazard: Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
December 17, 2025Medical DevicesFDA
C.R. Bard Inc recalls BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm, Ureteral Stent Kit REF 788426
Hazard: Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
December 17, 2025Medical DevicesFDA
C.R. Bard Inc recalls Bard InLay Optima Size: 6 Fr. x 14 cm, Ureteral Stent Kit REF 787614
Hazard: Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
September 24, 2025Medical DevicesFDA
C.R. Bard Inc recalls SureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray, REF: A942216
Hazard: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when it's natural rubber latex, or 2)Natural rubber latex with infection control coating, when it's silicone hydrogel with antimicrobial coating, or 3)Natural latex with infection control, when it's silicone hydrogel coated without antimicrobial coating, which may cause infection and/or local and/or systemic allergic reaction
September 24, 2025Medical DevicesFDA
C.R. Bard Inc recalls SureStep Foley Tray System Lubri-Sil I.C. Complete Care Infection Control Foley Catheter Tray, REF: A303414A
Hazard: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when it's natural rubber latex, or 2)Natural rubber latex with infection control coating, when it's silicone hydrogel with antimicrobial coating, or 3)Natural latex with infection control, when it's silicone hydrogel coated without antimicrobial coating, which may cause infection and/or local and/or systemic allergic reaction
September 24, 2025Medical DevicesFDA
C.R. Bard Inc recalls SureStep Foley Tray System Bardex I.C. Complete Care Infection Control Foley Catheter Tray, REF: A303316A
Hazard: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when it's natural rubber latex, or 2)Natural rubber latex with infection control coating, when it's silicone hydrogel with antimicrobial coating, or 3)Natural latex with infection control, when it's silicone hydrogel coated without antimicrobial coating, which may cause infection and/or local and/or systemic allergic reaction
September 3, 2025Medical DevicesFDA
C.R. Bard Inc recalls Bardex Lubri-Sil I.C. 400-series Temperature Sensing Silver/Hydrogel Coated All-Silicone Foley Catheter 5cc Balloon, REF
Hazard: Foley catheter may have an obstructed lumen, which may result in an inability to drain the bladder, of urine and may include pelvic or abdominal pain, flank pain, bladder dysfunction, obstructive uropathy, acute kidney injury and/or hydronephrosis.
July 9, 2025Medical DevicesFDA
C.R. Bard Inc recalls REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra
Hazard: Cather packaging may contain the incorrect French size.
July 9, 2025Medical DevicesFDA
C.R. Bard Inc recalls BD Heyman Follower Coude Tip for following sizes: 12Fr - REF:021312 14Fr - REF:021314, 16Fr - REF: 021316
Hazard: Cather packaging may contain the incorrect French size.
July 9, 2025Medical DevicesFDA
C.R. Bard Inc recalls BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr - REF:21112, 14Fr - REF: 21114, 20Fr
Hazard: Cather packaging may contain the incorrect French size.
May 28, 2025Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Single Intragastric Linton Balloon Tube, REF: 0092740
Hazard: Due to customer complaints, there is a potential for users to be unable to or find it difficult to remove the plastic plugs in order to inflate the gastric and/or esophageal balloons.
May 28, 2025Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate)REF: 0092300
Hazard: Due to customer complaints, there is a potential for users to be unable to or find it difficult to remove the plastic plugs in order to inflate the gastric and/or esophageal balloons.
May 28, 2025Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) REF: 0092110
Hazard: Due to customer complaints, there is a potential for users to be unable to or find it difficult to remove the plastic plugs in order to inflate the gastric and/or esophageal balloons.
May 28, 2025Medical DevicesFDA
C.R. Bard Inc recalls Bard Blakemore Esophageal-Nasogastric Tube (Adult) REF: 0092100
Hazard: Due to customer complaints, there is a potential for users to be unable to or find it difficult to remove the plastic plugs in order to inflate the gastric and/or esophageal balloons.
May 28, 2025Medical DevicesFDA
C.R. Bard Inc recalls Bard Minnesota Four Lumen Esophagogastric Tamponade Tube, REF:0092220 18 Fr. (6mm, 7/32"), 41" Length (104cm) with 8" (2
Hazard: Due to customer complaints, there is a potential for users to be unable to or find it difficult to remove the plastic plugs in order to inflate the gastric and/or esophageal balloons.
June 26, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard Medical SureStep Foley Tray System, 16 Fr., Catalog #A319416AM; and Bard Medical Bardex IC Complete Care Infection
Hazard: Some of the devices may function incorrectly resulting in no temperature display or erratic temperatures being displayed on the temperature monitoring devices.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Suction Connector with ENFit, REF EN0066000
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Nasogastric Sump Tube and PreVent¿ Anti-Reflux Filter and Lopez Valve¿ with ENFit, 18Fr., 48in Long, REF EN0056180
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Nasogastric Sump Tube and PreVent¿ Filter and Lopez Valve¿ with ENFit, 16Fr., 48in Long , REF EN0056160
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Nasogastric Sump Tube and PreVent¿ Filter and Lopez Valve¿ with ENFit, 14Fr., 48in Long, REF EN0056140
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Nasogastric Sump Tube and PreVent¿ Anti-Reflux Filter and Lopez Valve¿ with ENFit, 12Fr., 48in Long, REF EN0056120
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Lopez Valve¿ with ENFit, REF EN0056000
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 18Fr., 48in Long, REF EN0046180
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 16Fr., 48in Long, REF EN0046160
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 14Fr., 48in Long, REF EN0046140
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit", 12Fr., 48in Long, REF EN0046120
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 10Fr., 36in Long, REF EN0046100
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ PreVent¿ Anti-Reflux Filter with ENFit, REF EN0046000
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.