Cook recalls Echosight Jansen-Anderson Intratubal Transfer Set (K-J-JITS-572900) due to incomplete quality testing that may cause nonviable embryos or gametes. Affected lots include specific serial numbers.
Certain lots of in vitro fertilization (IVF) products were distributed without completed finished device quality testing with potential adverse events that may include nonviable gametes and/or nonviable embryos.
Cook is recalling a specific IVF transfer set used in fertility treatments because some batches were made without proper quality testing. This could lead to nonviable embryos or gametes, potentially affecting fertility outcomes.
The IVF transfer set was distributed without completed quality testing, which could result in nonviable gametes or embryos. This means the fertility treatment might not work as intended, leading to unsuccessful pregnancies.
Women undergoing in vitro fertilization (IVF) treatments who used the recalled Echosight Jansen-Anderson Intratubal Transfer Set with the specific catalog number K-J-JITS-572900 are most at risk. The recall applies to specific lots manufactured with the lot number 7131328.
Check for the catalog number K-J-JITS-572900 and global product number G17946 on the device. The affected lot number is 7131328, with an expiration date of July 19, 2019.
Look for the catalog number K-J-JITS-572900 and global product number G17946 on the Echosight Jansen-Anderson Intratubal Transfer Set.
Cook recalls this IVF transfer set because certain lots were distributed without completed quality testing, which could lead to nonviable gametes or embryos.
Check the catalog number and lot number on the device. If it matches the recalled items (K-J-JITS-572900 and lot 7131328), contact Cook for further instructions.
The recall is for potential nonviable embryos or gametes, not physical injury. The hazard level is low risk as it does not involve immediate physical harm.
We’ve drafted a message you can send Cook to request your refund or repair — edit it as you like.
Subject: Recall Z-1186-2018 — Cook Cook Hello, I own a Cook that is covered by recall Z-1186-2018 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.
