Device recall

Z-1531-2013: VIA Medical Collection Bag; The collection bag is an accessory waste bag used in…

FDA device recall · Class II · International Biomedical, Ltd.

Key facts

Recall number (Z-number) Z-1531-2013
Recall event 65341
Product VIA Medical Collection Bag; The collection bag is an accessory waste bag used in conjunction with the sterile LVM blood gas sensor with the LVM Monitor. The collection bag is packaged in a tyvek pouch which is included in either replacement kit (777-3103) or LVM sensor kit (777-3102).
Product code LZF
Recalling firm International Biomedical, Ltd.
Recall class Class II
Status Terminated
Termination date Jul 29, 2013
510(k) numbers K922997
FEI number 1000058335

At a glance

  • 1–9 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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