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

Recall Z-1553-2015 — Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number: 532.021 for orthopedic surgery.

U.S. FDA — Device Enforcement · United States · 2015-03-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1553-2015
Date of alert
2015-03-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
The Anspach Effort, Inc.
Product category
device
Product type
Devices
Reported risk: The potential exists for the Oscillating Saw Attachment to disengage from the Small Battery Drive handpiece. If the attachment disengages from the handpiece intra-operatively, there is a potential for injury to the patient and/or user.
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.

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