Device recall

Z-2558-2014: CollectEVAC, Sterile device with tubing and adaptor for use with ACMI and…

FDA device recall · Class II · Civco Medical Instruments Inc

Key facts

Recall number (Z-number) Z-2558-2014
Recall event 68951
Product CollectEVAC, Sterile device with tubing and adaptor for use with ACMI and STORZ/Wolf resectoscopes. Part number 610-954. Rx only. Sterile EO. The product is intended to be used to perform irrigation, tissue collection, and/or straining functions during transurethral prostate or bladder surgery.
Product code KQT
Recalling firm Civco Medical Instruments Inc
Recall class Class II
Status Terminated
Termination date Jan 28, 2015
FEI number 1937223

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

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