Sun Med recalls adult manual resuscitators with medium adult masks that may detach during use, risking air delivery issues. Affected units have specific 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 can interrupt air delivery to patients, which is critical in emergency medical situations.
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 CPRM1126P with lot numbers 313502 or 313741. These units were sold with specific reference numbers.
Identify the model number CPRM1126P and lot numbers 313:502 or 313741 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.
Check the model number CPRM1126P and lot numbers 313502 or 313741 to confirm if your device is affected. No specific action is required beyond checking.
The recall states there is a potential for the patient port to detach during use, which could interrupt air delivery. However, the remedy is not specified, so no immediate action is required beyond checking.
We’ve drafted a message you can send Sun Med to request your refund or repair — edit it as you like.
Subject: Recall Z-2158-2018 — Sun Med Sun Med Hello, I own a Sun Med that is covered by recall Z-2158-2018 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.
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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.
