If you developed a deep-joint infection after a hip or knee replacement in which a 3M Bair Hugger warming blanket was used, here is who may qualify in MDL 2666 — the surgical-device litigation the Eighth Circuit revived after it was first dismissed.
This page describes ongoing litigation and an investigation. The statements below are unproven allegations. 3M denies the allegations and disputes that the device causes infection; no company has been found liable, no settlement has been finalized, and eligibility depends on the facts of each case. This page is informational and is not legal or medical advice.
Plaintiffs allege that the 3M / Arizant Bair Hugger forced-air warming device, used to keep patients warm during surgery, disrupts sterile operating-room airflow and deposits airborne bacteria into open surgical sites — allegedly causing deep-joint (periprosthetic) infections in hip and knee replacement patients. These are unproven allegations, and 3M disputes them.
The claims generally involve patients who had a hip or knee replacement (or other orthopedic implant surgery) where a Bair Hugger forced-air warmer was used and who later developed a deep periprosthetic joint infection — sometimes requiring revision surgery, implant removal, prolonged antibiotics, or in severe cases amputation. Eligibility depends on the facts of each case.
The MDL court excluded the plaintiffs' general-causation experts and dismissed the cases around 2017 to 2019, but in August 2021 the Eighth Circuit Court of Appeals reversed that ruling and revived the litigation, and the U.S. Supreme Court declined to hear 3M's appeal in 2022. The cases returned to the MDL and remain active.
No. As of mid-2026 there is no global settlement. Court-supervised settlement discussions have continued under a special master, but no resolution has been announced and no claim form exists.
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