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Crosstex™

HU-FRIEDY MFG. CO., LLC · Model SP-GFS · UDI-DI 10889950134136

FYE
7
510(k) clearances
12
Adverse events
1
Recalls
119
Facilities

Description

Face Shield Sample Pack

Recalls

DateFirmReason
2013-05-08DePuy Orthopaedics, Inc.LifeLiner Stick and Cut Resistant Gloves are being recalled because cases and individual glove packages were mispackaged, with right handed, large sized glove packaging containing

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.