Digital Ultra Package B 56100Recalls & reported problems
Accutron, Inc. · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00813830023374), received between Apr 26, 2018 and Apr 26, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Gas/Air Leak” (1 report).
4 other recalls cover devices cleared under the same FDA submission (K052335); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Gas/Air Leak1
Patient problems
- Partial thickness (Second Degree) Burn1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 26, 2018Gas/Air Leak; Gas/Air Leak
A FACILITY REPORTED THAT THE ACCUTRON NITROUS MIXER UNIT CAUGHT FIRE AND INJURED A DENTAL ASSISTANT EMPLOYEE WHILE SWITCHING FROM FIRST OXYGEN TANK TO THE SECOND OXYGEN TANK.
Patient problems: Partial thickness (Second Degree) Burn
MAUDE report 7465840 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K052335. One submission often covers many models, so check the product and lot details in each record.
- Z-0018-2013 · Apr 29, 2012 · TerminatedUltra PC% Cabinet Mount Package G, Model #36600, Serial # 13593, 13594, 13595, 13596, 13597, 13598, 13599, 13600, 13602, 13605, 13610, 13611, 13612, 13615, 13616, 13617, 13621, 13
- Z-0019-2013 · Apr 29, 2012 · TerminatedCM Flowmeter Pkg H, Model #36700, Serial # 13749 Product Usage: Conscious Sedation Unit Analgesia Gas Machine.
- Z-0017-2013 · Apr 29, 2012 · TerminatedFlow Meter, CM Assembly, Model #27025, Serial # 13686, 13690, 13712, 13793. Flowmeter, CM Assembly, Model#31970, Serial#13692. Product Usage: Conscious Sedation Unit Analgesia
- Z-0020-2013 · Apr 29, 2012 · TerminatedNewport Portable Package, Model #50000, Serial # 13591, 13592, 13604, 13606, 13614, 13662, 13663, 13664, 13726, 13731, 13733, 13736, 13737, 13738, 13740, 13768, 13770, 13771, 1377
Other Gas-Machine, Anesthesia devices
- Carestation 650 A1Datex-Ohmeda Inc · Gas-machine, anesthesia2 recalls3,109 reports
- Carestation 750 A1Datex-Ohmeda Inc · Gas-machine, anesthesia2 recalls2,204 reports
- Aisys CS2Datex-Ohmeda Inc · Gas-machine, anesthesia5 recalls2,048 reports
- Carestation 620 A1Datex-Ohmeda Inc · Gas-machine, anesthesia2 recalls2,015 reports
- Avance CS2Datex-Ohmeda Inc · Gas-machine, anesthesia6 recalls1,540 reports
- Flow-c Anesthesia System 6887700Maquet Critical Care AB · Gas-Machine, Anesthesia6 recalls72 reports
- FLOW-i C20 6677200Maquet Critical Care AB · Gas-Machine, Anesthesia4 recalls99 reports
- Flow-e Anesthesia System 6887900Maquet Critical Care AB · Gas-Machine, Anesthesia5 recalls19 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.