Leica Microsystems, Inc. recalls Leica M530 OHX Microscope System Supplied with 100 - 120 Vac.
- Recall date
- June 25, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2659-2018
- FDA classification
- Class II
- Brand / firm
- Leica Microsystems, Inc.
- Sold / distributed
- United States distribution: AR, AZ, CA, CO, CT, DE, FL, IL, IN, KS, KY, LA, MO, NJ, NY, NV, OH, OR, PA, TX, UT, PR. International distribution to Japan, Brazil, Columbia, Ecuador, Mexico, Taiwan
Why it was recalled
Recall is due to a design weakness of the power insert module.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Leica M530 OHX Microscope System Supplied with 100 - 120 Vac.
Get recall alerts
Free email alert whenever Leica Microsystems, Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Leica Microsystems, Inc.