FDAAugust 7, 2024device

Essentia MAJ Laparotomy Std Pack, ESLT53B; Medical convenience kit

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

The hazard

ACS identified that due to an inoperable chart recorder, humidity readings were out-of-specification in one of the controlled environment areas. As a result, ACS is unable to confirm product sterilization assurance requirements were met.

What to do

FDA enforcement status: Ongoing

Brands named

american contract systemsamericanamerican contract

UPCs

00191072218438

Recall history

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

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