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Triton Canister Software Catalog Number: GAUS-2. Intended adjunct in the estimation of blood ...

FDA Recall #Z-1186-2023 — Class II — January 25, 2023

Recall #Z-1186-2023 Date: January 25, 2023 Classification: Class II Status: Ongoing

Product Description

Triton Canister Software Catalog Number: GAUS-2. Intended adjunct in the estimation of blood loss.

Reason for Recall

Triton Canister Software, Insert & Scanning Label may cause the Triton Canister System to output inaccurate blood loss estimates can lead to confusion and could potentially result in either delayed recognition or prolongation of postpartum hemorrhage (PPH), or require more aggressive treatment for PPH.

Recalling Firm

Stryker Corporation — Portage, MI

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

88 units

Distribution

US Nationwide distribution.

Code Information

UDI-DI: 00859506006029 Software Version: 2.8.4

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medical device immediately and consult your healthcare provider. Contact the recalling firm for instructions on return or replacement. If you experienced an adverse event, inform your doctor.

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