Cook recalls specific Percutaneous Pigtail Nephrostomy Sets due to risk of stiff wire guide tip entering patient during use. Affected units include Global Product Numbers G14094-G14899. Contact Cook for details.
The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip.
Cook is recalling certain Percutaneous Pigtail Nephrostomy Sets because the wire guide might be loaded incorrectly into its holder. This could cause the stiff tip of the wire guide to enter the patient instead of the flexible tip, potentially causing injury.
The wire guide may be incorrectly loaded into the wire guide holder, causing the stiff tip to enter the patient instead of the flexible tip. This could lead to injury during medical procedures.
Healthcare professionals using the Percutaneous Pigtail Nephrostomy Set for medical procedures are most at risk. Patients receiving this procedure may be affected if the device is used incorrectly.
Check for Global Product Numbers G14094, G14095, G14899, or G14329 on the device packaging. The specific model numbers 8112670, 8113259, 8113260, 8113261, NS8070847, and 8076035 are also affected.
Look for Global Product Numbers G14094, G14095, G14899, or G14329 on the device packaging.
The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip.
Check for Global Product Numbers G14094, G14095, G14899, or G14329 on the device packaging. The specific model numbers 8112670, 8113259, 8113260, 8113261, NS8070847, and 8076035 are also affected.
The recall record does not specify a remedy, so contact Cook directly for instructions.
We’ve drafted a message you can send Cook to request your refund or repair — edit it as you like.
Subject: Recall Z-0969-2020 — Cook Cook Hello, I own a Cook that is covered by recall Z-0969-2020 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.
