Accutron Inc: Medical Device Recall in 2012 - (Recall #: Z-0020-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Newport Portable Package, Model #50000, Serial # 13591, 13592, 13604, 13606, 13614, 13662, 13663, 13664, 13726, 13731, 13733, 13736, 13737, 13738, 13740, 13768, 13770, 13771, 13772, 13784, 13787. Product Usage: Portable Analgesia Gas Machine.

Product Classification:

Class I

Date Initiated: April 29, 2012

Date Posted: October 17, 2012

Recall Number: Z-0020-2013

Event ID: 63174

Reason for Recall:

Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it flows Nitrous Gas without Oxygen gas being turned on, it functions in an incorrect manner.

Status: Terminated

Product Quantity: 220 units total

Code Information:

Lot # 73656, 74139, 75209, 74689, 75515, 74858.

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated