Cook recalls HPCT8.8-120-M-FM connecting tubes for potential fluid leakage or air aspiration during angiography procedures. Affected lots listed in the recall notice.
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 certain connecting tubes used in angiography procedures due to a risk of fluid leakage or air entering the tube. This could cause complications during medical procedures if the tube isn't properly secured.
The cap-adapter assembly might not be tightened enough, which could allow fluid to leak out or air to enter the tube. This could lead to complications during medical procedures like contrast injections or pressure monitoring.
Healthcare professionals using the connecting tube during angiography procedures are most at risk. Patients receiving the tube for contrast injection or pressure monitoring may also be affected.
Check the lot numbers on the tube: 7797164, 7844038-7857500, 7863742-7863751, 7871644-7871647, 7881937-7881942, 7888498-7888507, 7917423-7917434, 7925136-7925140, 7940326-7940346, 7949048, NS7835002, NS7875343, NS7881929, NS7888468, NS7928016, NS7940350.
Identify the lot number on the connecting tube to see if it matches the listed affected lots.
The connecting tube is used in angiography procedures to link a fluid reservoir to a vascular catheter for contrast injection, pressure monitoring, or fluid infusion.
The cap-adapter assembly might not be tightened enough, potentially causing fluid leakage or air to enter the tube during medical procedures.
Check the lot number on the tube; affected lots include 7797164, 7844038-7857500, 7863742-7863751, and other specific numbers listed in the recall notice.
We’ve drafted a message you can send Cook to request your refund or repair — edit it as you like.
Subject: Recall Z-1756-2018 — Cook Cook Hello, I own a Cook that is covered by recall Z-1756-2018 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.
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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.
