Device recall

Z-1546-2018: Medi-Vac(TM) Flex Advantage(TM) Suction Canister Liner, Material Numbers: a) REF…

FDA device recall · Class II · Cardinal Health 200, LLC

Key facts

Recall number (Z-number) Z-1546-2018
Recall event 79702
Product Medi-Vac(TM) Flex Advantage(TM) Suction Canister Liner, Material Numbers: a) REF 6561-910C b) REF 6561-916K c) REF 6561-920C To remove blood and/or body fluids. These fluids may be suctioned during surgical procedures or other applications requiring the removal of built up fluids. The suction…
Product code GCX
Recalling firm Cardinal Health 200, LLC
Recall class Class II
Status Terminated
Termination date Nov 29, 2018
FEI number 3001236905

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

Browse all FDA device recalls (products)