Bacchus Vascular Inc Bacchus brand Trellis Plus, Peripheral Infusion System, 6.0 Fr Catalog Numbers: BAC TRR 006 140 10, BAC TRR 006 140 20 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Bacchus brand Trellis Plus, Peripheral Infusion System, 6.0 Fr Catalog Numbers: BAC TRR 006 140 10, BAC TRR 006 140 20
Brand
Bacchus Vascular Inc
Lot Codes / Batch Numbers
Lot Numbers: M02-50216, M02-50217, M02-50219, M02-50220, M02-50227, M02-50228, P02-30014, P02-30013
Products Sold
Lot Numbers: M02-50216, M02-50217, M02-50219, M02-50220, M02-50227, M02-50228, P02-30014, P02-30013
Bacchus Vascular Inc is recalling Bacchus brand Trellis Plus, Peripheral Infusion System, 6.0 Fr Catalog Numbers: BAC TRR 006 140 1 due to The device has the potential for fractures at the distal end during use.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The device has the potential for fractures at the distal end during use.
Recommended Action
Per FDA guidance
On 11/24/03, all consignees were notified via phone calls and/or on-site visit by the firm''s sales representative, informing them of the affected devices and providing instructions on the recall.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026