FDA Medical Device Recalls (openFDA)
Becton Dickinson Medical Systems: DT-DL60-1 W/Bifurcated
- Recall number
- Z-0073-06
- Recalling firm
- Becton Dickinson Medical Systems
- Product
- DT-DL60-1 W/Bifurcated
- Status
- Terminated
- Initiated
- 2005-07-01
- Posted
- 2005-10-21
- Terminated
- 2011-08-09
- Reason
- Device could permit an over-infusion of IV solutions during pressure monitoring procedures.
- Root cause
- Other
- Action
- Consignees were notified by letter on 8/22/2005 and told to immediately locate and quarantine all affected product for return to BD. Customer Recall Response Card was to completed and returned. For questions concerning the recall, call 800-453-4538 between 8AM and 5PM MST.
- Quantity
- 620 units
- Distribution
- Nationwide, including PR. VA facilities in OH, WA, NV and NY. No military or foreign distribution by US firm..
- Lot, serial or model codes
- Part Number 682147. Lot numbers 010019, 102055, 105054, 103029, 106054, 107040, 108079, 109045, 110042, 201072, 203025, 207529, 310143, 310147, 311166, 312127, 401042, 401589, 403069.
- 510(k) numbers
- ["K791844"]
- PMA numbers
- not on file
- Product code
- KRA
- Firm FEI
- 1710034
- Firm city
- Sandy
- Firm state
- UT
- 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