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MSI Precision Specialty Instruments

Med Saver, Inc. · Model 11-0001 · UDI-DI 00194613020002

OHW Prescription
0
510(k) clearances
0
Adverse events
1
Recalls
23
Facilities

Description

Ophthalmic Burr, 5 Per Package

Recalls

DateFirmReason
2016-10-12Bausch & Lomb, Inc.According to firm ( Bausch & Lomb, Inc. ) on June 17, 2016 a packaging operator notified his supervisor he had not placed the operating instruction into the last repackaging of SK

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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.