Reported Jan 20, 2016 · Terminated

Mercury Medical Neo-Tee T-Piece Resuscitator and T-Piece Circuit. The Neo-Tee T-Piece Resuscitator is a gas powered…

Mercury Enterprises, Inc. dba Mercury Medical

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Mercury Enterprises, Inc. dba Mercury Medical · 11300 49th St N · Clearwater, FL · 33762-4807

Is this the product you have?

  • Mercury Medical Neo-Tee T-Piece Resuscitator and T-Piece Circuit. The Neo-Tee T-Piece Resuscitator is a gas powered emergency resuscitator intended to provide emergency respiratory support by means of a face mask or a tube inserted into a patient's airway. It is intended for use with neonates and infants weighing less than 10kg (22 lb). The T-piece resuscitator circuit is a component used in conjunction with the T-piece resuscitator devices
Lot codes and dates

31 of 31 products

Products covered by this recall
Model / numberBarcodesProduct as published
105080010641043508004Unique Device ID # 10641043508004 Lot #s less than 1528850800
105080110641043508015Unique Device ID # 10641043508015 Lot #s less than 1528850801
105080210641043508022Unique Device ID # 10641043508022 Lot #s less than 1528850802
105080310641043508039Unique Device ID # 10641043508039 Lot #s less than 1528850803
105080410641043508046Unique Device ID # 10641043508046 Lot #s less than 1528850804
105080510641043508053Unique Device ID # 10641043508053 Lot #s less than 1528850805
105080610641043508060Unique Device ID # 10641043508060 Lot #s less than 1528850806
105080710641043508077Unique Device ID # 10641043508077 Lot #s less than 1528850807
105080810641043508084Unique Device ID # 10641043508084 Lot #s less than 1528850808
105080910641043508091Unique Device ID # 10641043508091 Lot #s less than 1528850809
105081010641043508107Unique Device ID # 10641043508107 Lot #s less than 1528850810
105081110641043508114Unique Device ID # 10641043508114 Lot #s less than 1528850811
105081210641043508121Unique Device ID # 10641043508121 Lot #s less than 1528850813
1050813810641043508004Unique Device ID # 10641043508004 Lot #s less than 1528850813
1050814Unique Device ID # 106410435081454 Lot #s less than 1528850814
105081510641043508152Unique Device ID # 10641043508152 Lot #s less than 1528850815
105081610641043508169Unique Device ID # 10641043508169 Lot #s less than 1528850816
105081710641043508176Unique Device ID # 10641043508176 Lot #s less than 1528850817
105081810641043508183Unique Device ID # 10641043508183 Lot #s less than 1528850818
105081910641043508190Unique Device ID # 10641043508190 Lot #s less than 1528850819
Amount recalled
753,245 devices

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Incorrect use of T-Piece resuscitators will result in complete occlusion of the patient circuit and consequent failure to ventilate the patient.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Oct 13, 2017 · Data as of Sep 19, 6:01 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.