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Radiesse

LAMBSMEAD LTD · Model 8071M5K1 · UDI-DI 05060457760082

MIX
10
510(k) clearances
41
Adverse events
1
Recalls
10
Facilities

Recalls

DateFirmReason
2015-10-26Merz North America, Inc.The expiration date encoded in the UDI barcode on the label on the product carton and the peelable patient identification label is incorrect.

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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.