C.r. Bard, Inc.
8195 INDUSTRIAL BLVD., COVINGTON, GA, US
Registered product codes
163 product codes
Recent MDR events
185,648 on file
- Power Port MRI isp, 8 Fr. Groshong, Int w SP, Attachable SLJul 31, 2026Injury3006260740-2026-05369
- Power Port MRI isp, 8 Fr. Groshong, Int w SP, Attachable SLJul 31, 2026Injury3006260740-2026-05371
- Implanted PortJul 31, 2026Malfunction3006260740-2026-05370
- GlidePathJul 31, 2026Malfunction3006260740-2026-05373
- 3DMaxJul 31, 2026Injury1213643-2026-00990
- Ventralight ST MeshJul 31, 2026Injury1213643-2026-00991
- Bard Soft MeshJul 31, 2026Injury1213643-2026-00992
- Titanium Implantable Port, ChronoFlex Single-Lumen, Kit, 8FJul 31, 2026Injury3006260740-2026-05382
- PowerPort isp M.R.I. Implantable Port, ChronoFlex Single-Lumen, 8FJul 31, 2026Injury3006260740-2026-05387
- PowerPort ClearVUE Slim Implantable Port, ChronoFlex Single-Lumen, Kit, 6FJul 31, 2026Injury3006260740-2026-05389
Recalls
130 on file
- Open, ClassifiedMay 21, 2026
Due to stain present on the surface of affected foley catheters.
View FDA record ↗ - Open, ClassifiedDec 11, 2025
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
View FDA record ↗ - Open, ClassifiedDec 11, 2025
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
View FDA record ↗ - Open, ClassifiedDec 11, 2025
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
View FDA record ↗ - Open, ClassifiedDec 11, 2025
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
View FDA record ↗ - Open, ClassifiedSep 18, 2025
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
View FDA record ↗ - Open, ClassifiedSep 18, 2025
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
View FDA record ↗ - Open, ClassifiedSep 18, 2025
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
View FDA record ↗ - Open, ClassifiedAug 28, 2025
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.
View FDA record ↗ - Open, ClassifiedJul 3, 2025
Cather packaging may contain the incorrect French size.
View FDA record ↗
Compliance history
Matched by FEI 1018233.
FDA inspections
2 on file
- No Action Indicated (NAI)Nov 12, 2024
Compliance: Devices
- No Action Indicated (NAI)Nov 12, 2024
Postmarket Assurance: Devices
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.