Device recall

Z-1140-2008: B-K Medical Intraoperative Transducer Type 8814, diagnostic ultrasound…

FDA device recall · Class II · B & K Medical Systems, Inc.

Key facts

Recall number (Z-number) Z-1140-2008
Recall event 46394
Product B-K Medical Intraoperative Transducer Type 8814, diagnostic ultrasound transducer, B-K Medical Systems, Inc., Wilmington, MA 01887
Product code IYN
Recalling firm B & K Medical Systems, Inc.
Recall class Class II
Status Terminated
Termination date Jun 23, 2008
510(k) numbers K024236, K043524
FEI number 1000305740

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 100–999 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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