Mercury Medical recalls pediatric Neo-Tee T-Piece Resuscitators with part numbers 1050805 and 1050832 due to risk of circuit controller detachment during use. Affected units sold with specific lot numbers.
Manual resuscitator circuit flow controller may come apart due to a missing manufacturing step.
Mercury Medical is recalling pediatric emergency resuscitators that may have a circuit controller that detaches. This could cause breathing issues for children in emergencies if the device fails during use.
The resuscitator's circuit flow controller might detach because of a missing manufacturing step. If it detaches during use, it could disrupt the air flow needed for emergency breathing support, potentially causing harm to a child.
Parents and caregivers of children using pediatric emergency respiratory support devices. Children in emergency situations are most at risk if the device fails.
Check the part numbers on the device: 1050805 or 1050832. Look for lot numbers 2417650805, 2417750805 for part 1050805 or 2423550832, 2417850832 for part 1050832.
Look for part numbers 1050805 or 1050832 on the device label.
Reach out to Mercury Medical for specific instructions on how to handle the device if it is affected.
The circuit flow controller may detach due to a missing manufacturing step, which could disrupt air flow during emergency use.
Part numbers 1050805 and 1050832 with specific lot numbers listed in the recall notice.
Check the part number on the device; affected units have part numbers 1050805 or 1050832 with specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Mercury Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0004-2025 — Mercury Medical Mercury Medical Hello, I own a Mercury Medical that is covered by recall Z-0004-2025 from Mercury Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
