Cook Medical recalls Blue Rhino G2 Multi Percutaneous Tracheostomy Introducer Sets with expiration dates exceeding true shelf life. Affected units include specific part numbers and lot numbers listed in the recall notice.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook Medical is recalling Blue Rhino G2 Tracheostomy Introducer Sets that have expiration dates longer than their actual shelf life. This could lead to product failure if used beyond the safe period, potentially causing complications for patients needing tracheostomy care.
The recalled devices have expiration dates that exceed the actual shelf life of the product. This means the devices could become ineffective or unsafe after the intended use period, potentially leading to complications for patients requiring tracheostomy care.
Healthcare professionals and patients who use tracheostomy devices may be affected. Those with the specific part numbers and lot numbers listed in the recall are most at risk.
Check for the part numbers C-PTIS-100-HC-G-EU, C-PTIS-100-HC-G-NA, C-PTIS-100-UNL-HC-G-EU, or C-PTIS-100-UNS-HC-G-EU. Also look for the specific lot numbers listed in the recall notice.
Identify your device's part number and lot number to see if it matches the affected units listed in the recall.
The product has expiration dates that exceed the true shelf life, which could lead to device failure after the intended use period.
Check for the specific part numbers and lot numbers listed in the recall notice to determine if your device is affected.
The recall does not specify a remedy, so contact Cook Medical directly for further instructions.
We’ve drafted a message you can send Cook Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1779-2026 — Cook Medical Cook Medical Hello, I own a Cook Medical that is covered by recall Z-1779-2026 from Cook 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.
