Cook recalls Pericardiocentesis Catheter Set RPN C-PCS-850 with potential small distal end hole. Affected units may cause complications during medical procedures. Contact Cook for remedy details.
Affected products may have been manufactured with the catheter distal end hole too small
Cook is recalling a specific pericardiocentesis catheter set due to a possible small hole at the distal end that could cause complications during medical procedures. This recall affects medical professionals using the product for heart fluid removal.
The catheter's distal end hole may be too small, potentially causing blockages or improper fluid drainage during pericardiocentesis procedures. This could lead to complications like fluid buildup or infection if the catheter doesn't function correctly.
Medical professionals who use the Cook Pericardiocentesis Catheter Set RPN C-PCS-850 for procedures like heart fluid drainage. Patients receiving this treatment are at risk if the catheter is used without proper verification.
Check for the model RPN C-PCS-850 and order number G03282 on the product packaging. Lot numbers include 7716007, 7703324, NS7703501, NS7703502, NS7703503, NS7704718, NS7704722, NS7704727, and NS7704728.
Verify the model number RPN C-PCS-850 and order number G03282 on the packaging to confirm if the product is affected.
The catheter distal end hole may be too small, potentially causing blockages or improper fluid drainage during medical procedures.
Lot numbers 7716007, 7703324, NS7703501, NS7703502, NS7703503, NS7704718, NS7704722, NS7704727, and NS7704728 are affected.
The recall record does not specify a remedy, so contact Cook directly for further instructions.
We’ve drafted a message you can send Cook to request your refund or repair — edit it as you like.
Subject: Recall Z-1722-2019 — Cook Cook Hello, I own a Cook that is covered by recall Z-1722-2019 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.
