Cook recalls HPCT8.8-60-M-FM-BNS connecting tubes for potential fluid leakage during angiography procedures. Affected units may cause air aspiration or fluid leakage if the cap-adapter assembly isn't properly tightened.
Cap-adapter assembly of the device may potentially not be adequately tightened, possibly leading to fluid leakage from or air aspiration into the connecting tube.
Cook is recalling a specific connecting tube used in angiography procedures because it might not stay securely tightened, which could cause fluid leakage or air entering the tube. This poses a risk during medical procedures where precise connections are critical.
The cap-adapter assembly might not be tightened enough, causing fluid to leak out of the tube or air to enter it. This could lead to improper fluid delivery or air embolism during medical procedures like angiography.
Healthcare professionals using the connecting tube during angiography procedures are most at risk. Patients receiving the tube for contrast injections or pressure monitoring may also be affected.
Check for the model number HPCT8.8-60-M-FM-BNS on the connecting tube. The product was sold for use in angiography procedures to connect contrast injectors and catheters.
Ensure the cap-adapter assembly is securely tightened before use to prevent fluid leakage or air aspiration.
The product may be safe if the cap-adapter assembly is properly tightened, but there is a risk of fluid leakage or air aspiration if not secured correctly.
The recall does not specify a return or replacement process; users should check the tightness of the cap-adapter assembly before use.
Patients receiving the tube for contrast injections or pressure monitoring could experience fluid leakage or air entering the system if the assembly isn't properly tightened.
We’ve drafted a message you can send Cook to request your refund or repair — edit it as you like.
Subject: Recall Z-1752-2018 — Cook Cook Hello, I own a Cook that is covered by recall Z-1752-2018 from Cook. 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.
