Device recall

Z-1852-2011: Large Port Specimen Sock, used to convert the pour/accessory port of a Cardinal…

FDA device recall · Class III · Cardinal Health Inc

Key facts

Recall number (Z-number) Z-1852-2011
Recall event 58028
Product Large Port Specimen Sock, used to convert the pour/accessory port of a Cardinal Suction canister into a specimen retainer. The sock is used as an accessory in a suction collection system. Its placed in a suction canister to remove solids from the liquid aspirated during surgery. The solids may…
Product code NNI
Recalling firm Cardinal Health Inc
Recall class Class III
Status Terminated
Termination date Oct 4, 2011
FEI number 3004008697

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 1–9 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

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