Product Liability Claim Solutions
Product Liability Litigation Support
Voluminous medical documentation in product liability cases doesn’t have to slow you down. We offer precision-driven medical record reviews for product liability claims, uncovering hidden insights.
8,500+
Product Liability Cases Analyzed
200+
Product Types Covered
96%
Causation Documentation Rate
48 Hours
Standard Case Turnaround
What Makes Our Medical Record Analysis Defensible
Our medical record review services for product liability are strongly built on precise analysis, clear clinical reasoning, and traceable evidence
Product Exposure & Usage Validation
Detailed analysis of medical records with a keen focus on product usage, dosage, duration, and conditions of exposure to establish connection with reported injuries.
Alternative Cause Identification
Assessment of comorbidities, prior injuries, and non-product factors in the medical records to distinguish product-related issues and pre-existing conditions.
Multi Plaintiff Coordination
Scalable product liability medical record analysis across multiple plaintiffs, aligning common defects, injury patterns, and exposure timelines to support causation.
Injury Pattern Analysis
Thorough evaluation of records to find out if clinical findings, diagnostic results, and treatment approaches are medically consistent with the alleged product defect.
Our Specialized Product Liability Solutions
We provide comprehensive medical record analysis services to support all types of product liability claims and defenses
Product-Specific Medical Chronologies
Detailed medical chronologies with special focus on product usage, installation dates, complications, revisions, and outcomes to support product liability causation arguments.
Product implantation tracking
Adverse event timeline
Revision/removal documentation
Injury Pattern Analysis & Data Extraction
Systematic extraction of key medical data points across different plaintiff pools—injury types, complication dates, product lot numbers, surgical details—to identify patterns and strengthen liability claims.
Cross-plaintiff pattern detection
Complication clustering
Lot number tracking
Medical Device & Implant Documentation
Specialized record review of operative reports, imaging studies, and device records that reflect medical device implantation procedures, device specifications, and failure.
Device model identification
Surgical technique review
Imaging analysis integration
Failure-to-Warn Evidence Review
Detailed review and analysis of patient education records, informed consent documents, and provider communications to support product liability claims with failure-to-warn and inadequate instruction.
Consent documentation review
Warning label analysis
Provider communication audit
Full-Spectrum Product Liability Case Analysis
Product Litigation Categories We Handle
We deliver consistent, case-ready medical record review services for all product categories
Medical Devices & Implants
Joint Replacements (Hip, Knee)
Surgical Mesh Products
IVC Filters & Cardiovascular Devices
Spinal Implants
Dental Implants
Pharmaceutical Products
Drug-Induced Injuries
Prescription Medication Complications
Over-the-Counter Product Harm
Vaccine Injury Claims
Consumer Products
Defective Medical Equipment
Personal Care Products
Household Products
Children's Products
Automotive & Industrial
Automotive Defects with Injury
Industrial Equipment Failures
Safety Equipment Malfunctions
Machinery-Related Injuries
Why Clients Choose Us
Top product liability firms tie up with us for our structured, defensible approach in product liability record review.
Investigation of all product-specific injury patterns in plaintiff populations of a claim
Supporting causation arguments with implantation and complication timelines
Systematic tracking of device lot numbers, model variations, and manufacturing dates
Product-focused summaries for streamlined expert witness preparation
Detection of failure modes and complication clusters for stronger litigation strategy
Expertise in medical devices, pharmaceuticals, automotive, & consumer products
Our Product Liability Expertise
Medical Device Specialists
FDA Regulatory Knowledge
Failure Mode Analysis Experience
Multi-Plaintiff Pattern Recognition
Our Product Liability Success Story
Hip Implant Product Liability
450 Plaintiffs
Challenge
Client law firm representing 450 plaintiffs with failed hip implants needed to identify common failure patterns, complication timelines, and revision surgery details to support design defect claims against manufacturers.
Solution
Created standardized chronologies capturing implantation dates, device specifications, complication onset, pain scores, imaging findings, and revision surgery details. Extracted structured data for pattern analysis across entire plaintiff population.
Results Achieved
450
Cases processed in 45 days
89%
Revision surgery cases within 5 years
6
Common failure patterns identified
$380M
Settlement achieved
Frequently Asked Questions
Got questions about our product liability litigation support services? We will clarify them here!
We specialize in medical device litigation, creating chronologies that capture device implantation dates, surgical details, device specifications (model, lot number, size), complication onset, imaging findings, and revision/removal procedures. Our team understands FDA classifications, recall histories, and device failure mechanisms.
Yes, that's one of our core strengths. We use standardized data extraction protocols to capture key variables across plaintiff populations—injury types, complication timelines, product lot numbers, failure modes—enabling pattern recognition and clustering analysis to strengthen your litigation strategy.
We support all major product liability categories including medical devices and implants, pharmaceutical litigation, defective consumer products, automotive defects with personal injury, and industrial equipment failures. Our team has experience with over 200 different product types.
We create detailed timelines linking product use/implantation to specific adverse events, complications, and injuries. Our chronologies include pre-implant health status, product installation details, symptom onset, diagnostic findings, and progression—providing clear temporal relationships to support causation arguments.
Absolutely. We systematically extract and document device identifiers including lot numbers, serial numbers, manufacturing dates, model variations, and device specifications from operative reports, device cards, and medical records. This information is critical for identifying defective batches and supporting manufacturing defect claims.
Yes. We identify documented misuse, deviations from instructions, or contraindications noted in the medical records that may impact liability arguments.
Yes. Our processes scale from single-plaintiff matters to high-volume MDLs without sacrificing consistency or quality.
Absolutely. We apply uniform review frameworks to ensure consistent injury analysis, exposure timelines, and reporting across all plaintiffs.
Yes. Our structured reviews identify medical strengths, weaknesses, and risk factors early—helping firms decide which claims to pursue.
Yes. We document treatment intensity, duration of care, complications, and long-term medical impact to support damages evaluation.

