Reported Jan 22, 2025 · Ongoing

Neo-Tee T-Piece Resuscitator, for pediatric emergency respiratory support, Part: 1050805, 1050808, 1050809, 1050810,…

Mercury Enterprises, Inc. dba Mercury Medical

High riskUsing this product could cause serious injury, illness or death — stop using it now.

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?

  • Neo-Tee T-Piece Resuscitator, for pediatric emergency respiratory support
  • Part
    • 1050805
    • 1050808
    • 1050809
    • 1050810
    • 1050811
    • 1050814
    • 1050832
    • 1050839
    • 1050840
    • 1050841
    • 1050842
Lot codes and dates

11 of 11 products · 58 lot codes

Recalled lot codes, grouped by product number
PartUDI-DI / Lot
1050805
  • 10641043508053
  • 30641043508057/2421450805
  • 2423550805
  • 2423650805
  • 2426750805
1050808
  • 10641043508084
  • 30641043508088/2426450808
  • 2426750808
  • 2426850808
  • 2429050808
  • 2429350808
1050809
  • 10641043508091
  • 30641043508095/2426450809
  • 2426750809
  • 2429050809
  • 2429150809
  • 2429350809
  • 2429750809
  • 2429850809
  • 2430050809
  • 2430250809
1050810
  • 10641043508107
  • 30641043508101/2426750810
  • 2429350810
  • 2429750810
  • 2429850810
  • 2430250810
1050811
  • 10641043508114
  • 30641043508118/2426550811
  • 2426650811
  • 2426750811
  • 2429050811
  • 2429150811
  • 2429250811
  • 2429350811
  • 2429450811
  • 2429750811
  • 2429850811
  • 2429950811
  • 2430250811
1050814
  • 10641043508145
  • 30641043508149/2426450814
  • 2426750814
  • 2429050814
  • 2429750814
  • 2430250814
1050832
  • 10641043508329
  • 30641043508323/2429050832
  • 242985083
1050839
  • 10641043508398
  • 30641043508392/2430350839
1050840
  • 10641043508404
  • 30641043508408/2429050840
  • 2429750840
1050841
  • 10641043508411
  • 30641043508415/2429050841
Amount recalled
37370

Where it was sold

Why it was recalled

Stop using this product now

Gas powered emergency resuscitator has a circuit flow controller manufactured with an undersized spring, which may cause resuscitator not reach the high and low ends of the PIP and PEEP pressure ranges, which may cause a loss of positive pressure, impacting effective ventilation of the patient.

Using this product could cause serious injury, illness or death — stop using it now.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:58 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.