FDA Device Intelligence
Home › Zimmer, Inc. › Miller™

Miller™

Zimmer, Inc. · Model 5069-52 · UDI-DI 00889024376670

JDYKIH Prescription
8
510(k) clearances
19
Adverse events
1
Recalls
20
Facilities

Recalls

DateFirmReason
2008-06-30Zimmer Inc.The cartridge is brittle and at increased risk of breakage.

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.