C.R. Bard recalls

C.R. Bard has 123 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 16 Sep 2026. 71 are still ongoing. 11 were reported in the last 12 months. The most frequent reason is sterility.

Total recalls123since 2014
Last 12 months11reported
Class I54% of total
Ongoing71latest 16 Sep 2026

Recalls per month, last 24 months

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Severity split

Class I 5 4%Class II 113 92%Class III 5 4%

By year

Ongoing c.r. bard recalls

71 active

All c.r. bard recalls, newest first

123 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIProducts that contain the Pericare Wipes: *Bardex¿ I.C recalledC.R. BardOtherNationwide
DeviceCLASS IIProducts that contain the Pericare Wipes recalled by C.R. BardC.R. BardOtherNationwide
DeviceCLASS IIProducts that contain the Pericare Wipes recalled by C.R. BardC.R. BardOtherNationwide
DeviceCLASS IIProducts that contain the Pericare Wipes recalled by C.R. BardC.R. BardTemperature AbuseNationwide
DeviceCLASS IIProducts that contain the Pericare Wipes recalled by C.R. BardC.R. BardTemperature AbuseNationwide
DeviceCLASS IIProducts that contain the Pericare Wipes recalled by C.R. BardC.R. BardOtherNationwide
DeviceCLASS IISilastic Foley Catheters Silastic Foley Catheter 30cc recalledC.R. BardOther44 states
DeviceCLASS IIBD InLay Optima Ureteral Stent Kit Size:., Ureteral Stent Kit recalledC.R. BardDevice MalfunctionNationwide
DeviceCLASS IIBD InLay Optima Ureteral Stent Kit Size: 4.., Ureteral Stent Kit recalledC.R. BardDevice MalfunctionNationwide
DeviceCLASS IIBard InLay Optima Size:., Ureteral Stent Kit recalled by C.R. BardC.R. BardDevice MalfunctionNationwide
DeviceCLASS IIBD InLay Optima Ureteral Stent Kit Size:., Ureteral Stent Kit recalledC.R. BardDevice MalfunctionNationwide
DeviceCLASS IISureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray recalledC.R. BardForeign MaterialNationwide
DeviceCLASS IISureStep Foley Tray System Lubri-Sil I.C. Complete Care recalledC.R. BardForeign MaterialNationwide
DeviceCLASS IISureStep Foley Tray System Bardex I.C. Complete Care recalledC.R. BardForeign MaterialNationwide
DeviceCLASS IIBardex Lubri-Sil I.C. 400-series Temperature Sensing recalledC.R. BardTemperature AbuseNationwide
DeviceCLASS IIBD Heyman Follower Coude Tip for following sizes recalled by C.R. BardC.R. BardPackaging DefectsNationwide
DeviceCLASS IIBD Heyman Follower Straight Tip for following sizes recalledC.R. BardPackaging DefectsNationwide
DeviceCLASS IIREF: 123400,Bard Urologist's Tray, For the Obstructed Urethra recalledC.R. BardPackaging DefectsNationwide
DeviceCLASS IBard Blakemore Esophageal-Nasogastric Tube (Adult) recalled by C.R. BardC.R. BardForeign Material44 states
DeviceCLASS IBard Minnesota Four Lumen Esophagogastric Tamponade Tube recalledC.R. BardForeign Material44 states
DeviceCLASS IBard¿ Blakemore Esophageal-Nasogastric Tube (Child) recalledC.R. BardForeign Material44 states
DeviceCLASS IBard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate) recalledC.R. BardForeign Material44 states
DeviceCLASS IBard¿ Single Intragastric Linton Balloon Tube recalled by C.R. BardC.R. BardForeign Material44 states
DeviceCLASS IIBard Medical SureStep Foley Tray System recalled by C.R. BardC.R. BardTemperature AbuseNationwide
DeviceCLASS IIBard¿ Nasogastric Sump Tube with ENFit recalled by C.R. BardC.R. BardOtherGA
DeviceCLASS IIBard¿ Nasogastric Sump Tube with ENFit recalled by C.R. BardC.R. BardOtherGA
DeviceCLASS IIBard¿ Nasogastric Sump Tube and PreVent¿ Filter recalled by C.R. BardC.R. BardOtherGA
DeviceCLASS IIBard¿ Nasogastric Sump Tube recalled by C.R. BardC.R. BardOtherGA
DeviceCLASS IIBard¿ Suction Connector with ENFit recalled by C.R. BardC.R. BardOtherGA
DeviceCLASS IIBard Nasogastric Sump Tube with ENFit recalled by C.R. BardC.R. BardOtherGA

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.