Sun Med recalls adult resuscitators with potential patient port detachment during use. Affected models include CPRM1116PD5 with specific lot numbers. No remedy provided in official notice.
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 detach during use, risking interrupted air delivery to patients. This could lead to inadequate patient care if the port becomes dislodged.
The patient port retaining ring may not fully seat, causing the port to detach during use. This can interrupt air delivery to the patient, potentially leading to inadequate ventilation.
Healthcare professionals using the recalled resuscitators are most at risk. Patients receiving care with these devices could experience interrupted air delivery.
Check for the model CPRM111:116PD5 with lot numbers 313326, 313436, or 313049. This resuscitator has a medium adult mask, bag reservoir, and 7 ft oxygen tubing.
Identify the model number and lot numbers to confirm if your device is affected.
The official recall notice does not provide a remedy.
Check the model number and lot numbers to see if your device is affected. No action is required if it is not listed.
Look for the model CPRM1116PD5 with lot numbers 313326, 313436, or 313049.
We’ve drafted a message you can send Sun Med to request your refund or repair — edit it as you like.
Subject: Recall Z-2151-2018 — Sun Med Sun Med Hello, I own a Sun Med that is covered by recall Z-2151-2018 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.
