National IVF Attorneys Provide Information on Who Qualifies to File an embryo loss lawsuit Against CooperSurgical

embryo loss lawsuit

In the realm of assisted reproductive technology, in vitro fertilization (IVF) represents a unique path for individuals and couples striving to conceive. However, amidst the promise of new life, there can be unforeseen challenges and setbacks. One such challenge arises when the very tools intended to facilitate the IVF process fail, leading to the devastating loss of embryos. This is the case with the CooperSurgical IVF culture media recall, prompting affected individuals to file embryo loss lawsuits against the company.

Embryo loss is a deeply distressing experience for those undergoing IVF treatment. It represents not only a physical loss but also an emotional and financial burden on individuals and couples already grappling with the complexities of infertility. When this loss is linked to defective or recalled products such as CooperSurgical culture media, it raises critical questions about accountability and recourse.

Individuals and couples who have experienced embryo loss due to the CooperSurgical IVF culture media recall are seeking clarification of the qualifications required to participate in an IVF embryo loss lawsuit. Our attorneys are dedicated to providing information and support to those considering filing a lawsuit related to this matter. On this page, we have compiled the basic qualifications our attorneys consider in each IVF loss lawsuit claim.

  • Use of CooperSurgical Culture Media: If you have undergone IVF treatment that utilized CooperSurgical culture media, you may be eligible to file a claim. CooperSurgical products are essential components in the IVF process. If your IVF treatment utilized CooperSurgical culture media and subsequently experienced embryo loss, you may have grounds for a lawsuit. Our attorneys can help assess your case and determine your eligibility for legal recourse.
  • Recalled Lots of Culture Media: Embryo loss can happen for a variety of reasons, but it was a widespread problem with three specific lots of CooperSurgical culture media that circulated the United States and Canada in November and December of 2023. The FDA CooperSurgical embryo solution recall included the following model numbers and lots of "global Medium": Model Numbers LGGG-020 (20mL bottle), LGGG-050 (50mL bottle), LGGG-100 (100mL bottle). The CooperSurgical IVF recall includes the following lots: LGGG-020: UDI-DI 00815965020044, lot 231020-018741; LGGG-050: UDI-DI 00815965020051, lot 231020-018742; LGGG-100: UDI-DI 00815965020068, lot 231020-018743.
  • Embryo Loss: and experienced embryo loss as a result of using CooperSurgical culture media, you may qualify to file a lawsuit. Embryo loss is a devastating outcome of the difficult and costly IVF process, and legal action may be warranted to seek justice and compensation.

For individuals and couples who meet these qualifications, it is likely you will be eligible to file an embryo loss lawsuit for the CooperSurgical IVF recall. There are multiple reasons to file a claim. First, IVF loss lawyers believe persons who lost embryos as a result of the defective culture media may be eligible for compensation for the loss as well as the expense of IVF treatment and associated suffering. More meaningful than that to some is the opportunity to hold a large corporation accountable for product safety and accountability. Critics say CooperSurgical made no effort to communicate with the people most affected by this recall, much less to compensate them for their losses.

Attorneys offering free, no obligation IVF embryo loss lawsuit case review are available to speak with you about your circumstances. To learn more about filing a lawsuit, please fill out the simple form linked on this page.


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Lawsuits for CooperSurgical IVF Recall Claims

Filing a lawsuit will allow you to hold the manufacturer accountable for embryo loss, while also providing real compensation for your expenses and suffering. Contact us today for a free consultation.