Sun Med recalls adult manual resuscitators with medium adult masks that may detach during use, risking air delivery issues. Affected units have 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 could detach during use, potentially interrupting air delivery to patients. This is a safety issue for healthcare providers using the device.
The patient port retaining ring may not fully seat, causing the port to detach during use. This could interrupt air delivery to the patient, potentially affecting their breathing.
Healthcare providers using the recalled resuscitators are most at risk. Patients receiving care with these devices could face interrupted air delivery.
Check for the model CPRM1116PC with lot number 313235. This product was sold with specific references and lot numbers.
Identify the model number CPRM1116PC and lot number 313235 to confirm if your device is affected.
The patient port retaining ring may not fully seat, causing the port to detach during use and potentially interrupting air delivery to patients.
The recall does not specify a remedy, so check the product details to confirm if it's affected and contact Sun Med for further instructions.
The recall states a potential for interrupted air delivery, but does not specify a risk of serious injury or death.
We’ve drafted a message you can send Sun Med to request your refund or repair — edit it as you like.
Subject: Recall Z-2150-2018 — Sun Med Sun Med Hello, I own a Sun Med that is covered by recall Z-2150-2018 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.
