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Sierra Wave

CADWELL INDUSTRIES, INC. · Model 190266-200 · UDI-DI 00840067100769

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510(k) clearances

Adverse events

Recalls

Facilities

Description

Amp-Stim Switch Box

Recalls

Date	Firm	Reason
2012-04-18	Biomet, Inc.	Incorrect product picture label was on the product box.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.