FDA Medical Device Recalls (openFDA)
Bard Medical Division: BARD SureStep Foley Tray System Bardex I.C. Complete Care Temperature Sensing Infection Control Foley Catheter with Bard Hydrogel and Bacteria-Guard Silver Alloy Coating. Sterile. Intended for use in the drainage and/or collection and/or measurement of urine.
- Recall number
- Z-0800-2019
- Recalling firm
- Bard Medical Division
- Product
- BARD SureStep Foley Tray System Bardex I.C. Complete Care Temperature Sensing Infection Control Foley Catheter with Bard Hydrogel and Bacteria-Guard Silver Alloy Coating. Sterile. Intended for use in the drainage and/or collection and/or measurement of urine.
- Status
- Open, Classified
- Initiated
- 2018-12-06
- Posted
- not on file
- Terminated
- not on file
- Reason
- Some SureStep" Foley Tray Systems with product catalog number A319418AM and lot number NGCT1929 contain vented sample ports that may have an increased likelihood of leaking urine from the vent on the sample port.
- Root cause
- Device Design
- Action
- Bard Medical Division notified customers on about 12/06/2018 via "MEDICAL DEVICE PRODUCT NOTIFICATION" letter. Customers were instructed to examine their inventory and identify any product subject to the recall, product return is not required, and if product was further distributed or transferred to notify those customers and include a copy of the medical device communication letter provided. Questions can be directed to Customer Service at 1-800-526-4455 or BMD.FieldAction@crbard.com.
- Quantity
- 450 units
- Distribution
- US Nationwide Distribution io KY, NE, GA, FL, MS, IN, IL, VA, OK, TX, NM, IL, VA, PA, CA, NV.
- Lot, serial or model codes
- Product Code A319418AM; Lot NGCT1929; Exp. Date 11/30/2018
- 510(k) numbers
- ["K910318"]
- PMA numbers
- not on file
- Product code
- MJC
- Firm FEI
- 1018233
- Firm city
- Covington
- Firm state
- GA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28