Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0930-2013 — ACUSON S2000 Automated Breast Volume Scanner (ABVS); Model number 10042541 Distributed by Siemens Medical Solutions USA Inc. business Unit: Ultrasound. The S2000 Automated Breast Volume Scanner (ABVS) Ultrasound System for imaging of the breast allows volumetric acquisition of the breast imag

U.S. FDA — Device Enforcement · United States · 2013-01-18 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0930-2013
Date of alert: 2013-01-18
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Siemens Medical Solutions USA, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10042541

Reported risk: On some ACUSON S2000 ABVS systems, the inside of the transducer pod may contain sharp edges.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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