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MR8

MEDTRONIC POWERED SURGICAL SOLUTIONS · Model MR8-12MH30SH · UDI-DI 00763000714642

HXZ ERL HBE HSZ HBC HBB Prescription

510(k) clearances

510

Adverse events

Recalls

246

Facilities

Description

TOOL MR8-12MH30SH 12CM MATCH 3MM SHORT

Recalls

Date	Firm	Reason
2020-11-20	Zimmer Biomet, Inc.	Device has the potential for fracture during use.

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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.