Sun Med recalls adult manual resuscitators with potential patient port detachment during use. This could affect air delivery to patients. Affected units include specific model and lot numbers.
There is a potential for the patient port retaining ring to not fully seat allowing the patient port to detach during use. This may impact air delivery to the patient.
Sun Med is recalling adult manual resuscitators that may have a patient port that detaches during use, which could impact air delivery to patients. This recall affects specific model numbers and lot numbers listed in the notice.
The patient port retaining ring might not fully seat, causing the port to detach during use. This could interrupt air delivery to the patient, potentially affecting their breathing.
Healthcare professionals using the recalled resuscitators are most at risk. Patients receiving care with these devices could be affected if the port detaches.
Check for the model number CPRM1126FP on the device. Affected units include lot numbers: 313323, 313355, 313739, 313031, 313093, 313190, and 313272.
Look for the model number CPRM1126FP on the resuscitator.
Confirm if your unit has one of the affected lot numbers: 313323, 313355, 313739, 313031, 313093, 313190, or 313272.
The model number is CPRM1126FP.
Affected lot numbers are 313323, 313355, 313739, 313031, 313093, 313190, and 313272.
The patient port may detach during use, which could interrupt air delivery to the patient and affect their breathing.
We’ve drafted a message you can send Sun Med to request your refund or repair — edit it as you like.
Subject: Recall Z-2156-2018 — Sun Med Sun Med Hello, I own a Sun Med that is covered by recall Z-2156-2018 from Sun Med. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.