C.R. Bard recalls
13 official recalls and safety alerts involving C.R. Bard since 2022-03, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with C.R. Bard or the relevant agency.
- 2026-09-16
USC.R. Bard Inc recalls Products that contain the Pericare Wipes: SureStep" Foley Tray System Add-A-Foley Catheter REF: A153200 UDI code: 00801741121067¿…
Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.
FDA · DeviceC.R. Bard IncWorldwide - U.S. Nationwide distribution including in the states of AK, AL,…Official notice →- 2026-05-27
- US
C.R. Bard Inc recalls Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley Catheter 5cc REF:…
Due to stain present on the surface of affected foley catheters.
FDA · DeviceC.R. Bard IncU.S.: AK, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD,…Official notice → - 2025-12-17
- US
C.R. Bard Inc recalls BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm, Ureteral Stent Kit REF 788630
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
FDA · DeviceC.R. Bard IncWorldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, GA,…Official notice → - 2025-09-24
- US
C.R. Bard Inc recalls SureStep Foley Tray System Bardex I.C. Complete Care Infection Control Foley Catheter Tray, REF: A303316A
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,…
FDA · DeviceC.R. Bard IncUS Nationwide distribution including in the states of NC, FL, NY, MA, MN, TX,…Official notice → - 2025-09-03
- US
C.R. Bard Inc recalls Bardex Lubri-Sil I.C. 400-series Temperature Sensing Silver/Hydrogel Coated All-Silicone Foley Catheter 5cc Balloon, REF: 119314; SureStep…
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…
FDA · DeviceC.R. Bard IncWorldwide - US Nationwide distribution in the states of IA, PA, AR, OR, MN,…Official notice → - 2025-07-09
- US
C.R. Bard Inc recalls REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra
Cather packaging may contain the incorrect French size.
FDA · DeviceC.R. Bard IncWorldwide - US Nationwide distribution including in the states of AL, AR, AZ,…Official notice → - 2025-05-28
- US
C.R. Bard Inc recalls Bard¿ Single Intragastric Linton Balloon Tube, REF: 0092740
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.
FDA · DeviceC.R. Bard IncUS: AK AL AR AZ CA CO CT DC DE FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO…Official notice → - 2024-06-26
- US
C.R. Bard Inc recalls Bard Medical SureStep Foley Tray System, 16 Fr., Catalog #A319416AM; and Bard Medical Bardex IC Complete Care Infection Control…
Some of the devices may function incorrectly resulting in no temperature display or erratic temperatures being displayed on the temperature monitoring devices.
FDA · DeviceC.R. Bard IncDistribution was nationwide. There was no government/military/foreign…Official notice → - 2024-01-31
- US
C.R. Bard Inc recalls Bard¿ Nasogastric Sump Tube with ENFit, 14Fr., 48in Long, REF EN0042140
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.
- 2023-12-20
- US
C.R. Bard Inc recalls Sensica Urine Output System, Catalog Number SCCS1002
BD (C.R. Bard) has received user complaints reporting that when the device was connected to WiFi/Internet, the time displayed on the Sensica device changed during a patient monitoring session which resulted in 1)…
- 2023-06-14
- US
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) REF 71816, f) REF…
Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility.
- 2022-07-06
- US
C.R. Bard Inc recalls Sensica Urine Output System
Complaints relating to urine output measurement accuracy.
- 2022-03-02
- US
C.R. Bard Inc recalls BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C
There is a potential to leak from the catheter where it connects to the drain bag
FDA · DeviceC.R. Bard IncUS Nationwide distribution in the states of GA, ME, NJ, WI, MN, SD, CO, ND,…Official notice →