Accutron, Inc.
1625 W Pinnacle Peak Rd, PHOENIX, AZ, US
Registered product codes
13 product codes
Recent MDR events
36 on file
- ULTRA DC FLOWMETERApr 3, 2026Injury2020813-2026-00002
- FLOWMETER, DIGITAL FLUSHMOUNTMar 19, 2026Injury2020813-2026-00001
- DIGITAL ULTRA FLUSHMOUNT PACKAGE HNov 21, 2025Injury2020813-2025-00010
- FLOWMETER, DIGITAL FLUSHMOUNTNov 6, 2025Injury2020813-2025-00009
- FLOWMETER, CMAug 25, 2025Injury2020813-2025-00008
- FLOWMETER, DIGITAL FLUSHMOUNTAug 11, 2025Injury2020813-2025-00006
- ULTRA DC FLOWMETERAug 8, 2025Injury2020813-2025-00005
- FLOWMETER, DIGITAL FLEXMOUNT, WALL ARMAug 8, 2025Injury2020813-2025-00007
- FLOWMETER, CMJun 27, 2025Injury2020813-2025-00004
- UNKNOWNMay 23, 2025Injury2020813-2025-00003
Recalls
4 on file
- TerminatedOct 9, 2012
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.
View FDA record ↗ - TerminatedOct 9, 2012
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.
View FDA record ↗ - TerminatedOct 9, 2012
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.
View FDA record ↗ - TerminatedOct 9, 2012
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.
View FDA record ↗
Compliance history
Matched by FEI 2020813.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.