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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
| Date | Firm | Reason |
|---|---|---|
| 2016-10-12 | Bausch & 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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Get your free API keyRead the docsData 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.
