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Pivotal Health Solutions, Inc. recalls Decompression Table Model E9011. This device applies cervical and/or lumbar decompression with practitioner definable ta
Recalled July 17, 2024 · FDA recall Z-2326-2024 · Pivotal Health Solutions
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. · FDA Class II
Units
32 tables
Sold at
Distributed to CA, FL, TX, ID, GA, and TN
Description
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.
Product
Decompression Table Model E9011. This device applies cervical and/or lumbar decompression with practitioner definable target treatment location, treatment pounds, and patterns of treatment.
Manufacturer(s)
Pivotal Health Solutions, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →