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

Recall Z-2784-2016 — Adaptor for Small Battery Drive and Small Battery Drive II. Product Usage: The Light Adaptor for Small Battery Drive (SBD) /Small Battery Drive II (SBD II) is designed for use in traumatology and orthopedic surgery of the skeleton, i.e. drilling, reaming or cutting bone. The Adaptors (05.001.024

U.S. FDA — Device Enforcement · United States · 2016-06-24 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2784-2016
Date of alert: 2016-06-24
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: The Anspach Effort, Inc.
Product category: device
Product type: Devices

Reported risk: There was a potential for the Adaptor and Light Adaptor for Small Battery Drive and Small Battery Drive II to generate excessive internal pressure that may cause the products to burst.

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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