Atlas FDA

Tri-State Hospital Supply Corp., Tri-State Centurion Venous Access Port Kits, Qty/case 20, sterile, Code No./Reorder KNV

FDA device recall Z-1571-2009 · posted 2009-07-07 · Terminated

Recall details

Recalling firm
Tri-State Hospital Supply Corporation
Reason for recall
The kits contain Monoject prefill heparin lock flush syringes, which were recalled by the manufacturer due to contamination.
Action taken
Tri State Hospital notified their consignees by letter dated 4/8/08 and instructed to discontinue use of the product and to either discard or return it.
Root cause
Material/Component Contamination
Status
Terminated
Product code
OKE
Quantity affected
100 kits
Distribution
Indiana, Mississippi, Ohio and Tennessee.
Date initiated
2008-04-08
Date posted
2009-07-07
Date terminated
2009-11-19
Location
Howell, MI

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