The Cooper Surgical IVF Fluid Recall Explained
In the complex world of assisted reproduction, embryo culture media serves as the artificial environment where embryos develop during their first critical days. These specialized fluids contain precisely balanced nutrients, growth factors, and antibiotics designed to mimic the natural conditions of a woman’s reproductive tract while supporting embryo development outside the body.
In December 2023, Cooper Surgical issued an urgent recall for three specific lots of their embryo culture media after discovering dangerous contamination with endotoxins—bacterial toxins that are highly toxic to developing embryos. This contamination essentially poisoned the very environment meant to nurture new life.
The recalled products include:
- LGGG-020: UDI-DI 00815965020044, lot 231020-018741
- LGGG-050: UDI-DI 00815965020051, lot 231020-018742
- LGGG-100: UDI-DI 00815965020068, lot 231020-018743
For Louisiana families whose fertility clinics used these contaminated lots, the consequences have been devastating. Clinical reports indicate that fertility centers experienced unprecedented embryo development failure rates—approaching 100% in some cases—when using the affected media. The FDA designated this a Class I recall, their most serious classification, indicating that exposure to these products may cause serious adverse health consequences or death of embryos.
Reproductive endocrinologists and embryologists confirm that endotoxin contamination is catastrophic for embryo development. When embryos are exposed to these bacterial toxins, they typically fail to develop properly, arresting growth and resulting in complete IVF cycle failure. For many Louisiana patients, this meant the loss of all viable embryos they had produced during their treatment cycle.
The situation is especially heartbreaking for patients who may have been using their final retrievable eggs due to age or medical conditions, potentially closing their window for biological parenthood permanently.
THE HUMAN IMPACT OF CONTAMINATED IVF MEDIA
Louisiana fertility clinics reported near-total embryo failure when using contaminated media, destroying all potential embryos from affected treatment cycles.
For women with age-related fertility decline or diminished ovarian reserve, the contaminated cycle may have been their last opportunity for genetic children.
Families experience profound grief after learning their reproductive hopes were destroyed by products meant to nurture their embryos.
Louisiana patients typically invest $15,000-$30,000 per IVF cycle, often from personal savings or loans, with little hope of reimbursement
Women endured intensive hormone protocols and invasive egg retrieval procedures, risking their health for cycles compromised by contaminated products.
These impacts represent just some of the hardships faced by Louisiana families affected by Cooper Surgical’s defective IVF media. Our Cooper Surgical IVF fluid lawyers at Dudley DeBosier Injury Lawyers understand that no compensation can truly replace lost opportunities to create your family, but we believe holding these companies accountable is an essential step toward justice.
Legal Foundations for Cooper Surgical IVF Claims
Cooper Surgical distributed embryo culture media containing dangerous contaminants, creating a defective product that destroyed developing embryos.
Evidence suggests Cooper Surgical neglected to implement proper quality control measures that would have detected the contamination before distribution.
By selling contaminated embryo culture media, Cooper Surgical breached implicit and explicit guarantees that their products were safe for their intended purpose.
The company appears to have delayed notification about contamination issues, potentially allowing more embryos to be exposed to defective media.
The emerging Cooper Surgical IVF fluid litigation draws on established product liability principles that protect consumers from defective medical products. In similar cases involving fertility treatment products, courts have recognized the unique harm suffered when reproductive opportunities are permanently lost due to product failures.
Current lawsuits seek compensation for both economic damages—including the substantial costs of failed IVF treatments—and non-economic damages such as emotional distress and loss of reproductive opportunity. These cases aim to hold Cooper Surgical accountable for apparent quality control failures in manufacturing these critical medical products.
At Dudley DeBosier Injury Lawyers, our Louisiana Cooper Surgical IVF fluid attorneys have extensive experience with complex medical product liability cases. We’re closely monitoring developments in this litigation and are prepared to advocate aggressively for the full compensation our clients deserve.
Do You Qualify for a Cooper Surgical IVF Lawsuit?
If you underwent IVF treatment in Louisiana between late 2022 and early 2024 and experienced an unexpectedly failed cycle, you may have grounds to file a claim against Cooper Surgical. Our Louisiana Cooper Surgical IVF fluid attorneys are helping families determine their eligibility and pursue appropriate compensation.
You may qualify for a Cooper Surgical IVF lawsuit if:
- You underwent IVF treatment that failed between approximately late 2022 and early 2024
- Your fertility clinic used embryo culture media from one of the recalled 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
- You experienced abnormal embryo development failure or unexpected poor outcomes
- You received notification from your clinic about the Cooper Surgical recall, or have reason to believe your clinic used affected products
- You have documentation of your IVF treatment including dates, procedures, and outcomes
Even if you’re uncertain whether your Louisiana fertility clinic used the recalled media, our Cooper Surgical IVF fluid lawyers can help investigate. Many clinics are now reviewing their records and contacting affected patients, but some families may remain unaware that their failed cycle was caused by contaminated products rather than natural causes.
The impact of contaminated culture media can manifest at different stages of IVF treatment. Whether your embryos failed to develop properly in the laboratory, failed to implant after transfer, or resulted in early pregnancy loss, defective media may have been the underlying cause.
At Dudley DeBosier Injury Lawyers, we understand the deeply personal nature of these cases and approach each client with compassion while aggressively pursuing the compensation they deserve.
Next Steps for Louisiana Families
Contact your fertility clinic to confirm if they used any recalled Cooper Surgical media during your treatment and request complete documentation.
Gather all materials related to your IVF treatment, including consent forms, lab reports, bills, and communications about the recall.
Connect with counseling services experienced in reproductive loss while exploring your legal options for accountability and compensation.
Speak with our Louisiana Cooper Surgical IVF fluid attorneys promptly, as time limits restrict how long you have to pursue your claim.
At Dudley DeBosier Injury Lawyers, we recognize that pursuing legal action may feel overwhelming when you’re already processing the emotional impact of a failed IVF cycle. Our compassionate Louisiana Cooper Surgical IVF attorneys will guide you through each step with sensitivity while fighting for the compensation you deserve.
Verify Your Eligibility Today
If your Louisiana IVF treatment failed due to contaminated Cooper Surgical embryo culture media, you deserve justice. Dudley DeBosier Injury Lawyers’ experienced Cooper Surgical IVF fluid attorneys are ready to evaluate your case and help you understand your options for compensation.
Time limits apply to these claims, and acting promptly gives you the best chance at recovery. Take the first step toward accountability today.
