Medical device recalls Moderate risk

Philips Electronics North America Corporation recalls UNIQ 1.0: UNIQ FD10, 722026; UNIQ FD10/10, 722027; UNIQ FD20, 722028; UNIQ FD20/10 biplane, 722029; UNIQ FD10 OR Table,…

Recall date
July 7, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2670-2016
FDA classification
Class II
Brand / firm
Philips Electronics North America Corporation
Sold / distributed
Nationwide, Canada, Algeria Argentina Australia Austria Bahrain Bangladesh Belgium Brazil Brunei Darussalam Bulgaria CHILE China Colombia Croatia Cuba Cyprus Czech Republic Denmark Dominican Republic Ecuador Egypt Finland France French Polynesia Georgia Germany Greece Honduras Hong Kong Hungary Ice…

Why it was recalled

Increase in the failure rate of certain low-voltage DC power supplies (DCPS)

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

UNIQ 1.0: UNIQ FD10, 722026; UNIQ FD10/10, 722027; UNIQ FD20, 722028; UNIQ FD20/10 biplane, 722029; UNIQ FD10 OR Table, 722033; UNIQ FD10/10 OR Table, 722034; UNIQ FD20 OR Table, 722035; UNIQ FD20/20, 722038; UNIQ FD20/20 biplane OR Table, 722039; UNIQ FD20/15, 722058; UNIQ FD20/15 OR Table 722059

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