RegWardenFDA facility compliance records
Recall

Class II — Precision Medical, Inc.

Recalling firmPrecision Medical, Inc
Registered facilityPRECISION MEDICAL, INC. (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonThese lots of Oxygen Dial Regulators could have the settings label off by one position. When the indicator arrow points to OFF position, the regulator is actually on the half liter setting (0.50), for the 15 liter. For the 8 liter, instead of being in the OFF position, the regulator will be in the quarter liter setting (0.25).
ProductEasy Dial Oxygen Regulator, 168708D and 168715D. Eight liter from .0.25 to 8 liters, 15 liter from 0.5 liter to 15 liters of oxygen per minute.
Quantity315
DistributionDistributed in the US to the states of PA, MA, MO, MT, ID, MI, MN, ND, KY, NY, NC, CA, AL, AZ, LA, OH, TX, GA, IN, and OK.
Initiated2015-10-08
Classified2015-11-13
Terminated2016-10-27
Recall numberZ-0272-2016
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Precision Medical, Inc. (Z-0272-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/72449/

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