Device recall

Z-1561-2010: PM1000 Flow Selector - An accessory to an emergency ventilator (resuscitator)…

FDA device recall · Class II · Precision Medical, Inc.

Key facts

Recall number (Z-number) Z-1561-2010
Recall event 55117
Product PM1000 Flow Selector - An accessory to an emergency ventilator (resuscitator). The selector is attached to a flowmeter and is used to direct the outlet flow from any standard flowmeter to any one of the three outlets it provides.
Product code BTM
Recalling firm Precision Medical, Inc.
Recall class Class II
Status Terminated
Termination date Dec 13, 2010
510(k) numbers K843223
FEI number 2523148

At a glance

  • 1–9 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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