Cook recalls Percutaneous Gastrojejunostomy Sets with potentially backward-loaded wire guides that could cause injury during catheter placement.
Cook has identified that the affected lots may contain wire guides that were loaded backwards into the wire guide holder.
Cook is recalling certain Percutaneous Gastrojejunostomy Sets that may have wire guides loaded backwards. This could lead to injury during catheter placement procedures.
The wire guides may be loaded backwards into the holder, which could cause improper catheter placement. This might lead to complications during gastroenteric feeding procedures.
Healthcare professionals using the device for gastroenteric feeding procedures. Patients receiving treatment through this device are at risk if the wire guides are misaligned.
Check the lot number on the device, which should be NS7587941 for the affected units. The product is intended for percutaneous placement of feeding catheters.
Look for the lot number NS7587941 on the device packaging or label.
The affected lots may contain wire guides that were loaded backwards into the wire guide holder.
Check the lot number on the device, which should be NS7587941 for the affected units.
The recall 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-0831-2018 — Cook Cook Hello, I own a Cook that is covered by recall Z-0831-2018 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.
