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Conformis, Inc. recalls iTotal Posterior Stabilized (PS) Knee Replacement System, Catalog Number TPS-111-1111 - 020102
Recalled April 10, 2019 · FDA recall Z-1079-2019 · Conformis
Hazard
The labeling of the boxes and sterile pouches did not match the contents. · FDA Class II
Units
2
Sold at
The products were distributed to the following US states: NH. The products were distributed to the following foreign countries: Germany
Description
The labeling of the boxes and sterile pouches did not match the contents.
Product
iTotal Posterior Stabilized (PS) Knee Replacement System, Catalog Number TPS-111-1111 - 020102
Manufacturer(s)
Conformis, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →