FDAApril 29, 2024device

Decompression Table Model E9011. This device applies cervical and/or lumbar decompression with practitioner definable target treatment location, treatment pounds, and patterns of treatment.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

This product is being recalled due to potentially insufficient rework on a part (E7130-B) on the lumbar section of the frame on 6 distributed tables. There were 4 additional tables with the faulty E7130-B part that were manufactured, but had not been distributed yet.

What to do

FDA enforcement status: Ongoing

Brands named

pivotal health solutionspivotalpivotal health

UPCs

00850008449826

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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