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Thermo Scientific

Thermo Electron LED GmbH · Model SL1R Plus-MD · UDI-DI 10850033408024

JQC
10
510(k) clearances
592
Adverse events (5 deaths)
16
Recalls
164
Facilities

Description

SL1R Plus-MD 220-230V/ 50/60Hz

Recalls

DateFirmReason
2019-02-06LW Scientific, Inc.The clear, plastic, polycarbonate hematocrit rotor may break apart during use and be ejected through the plastic housing, posing a safety hazard to the technician and potentially d
2019-02-06LW Scientific, Inc.The clear, plastic, polycarbonate hematocrit rotor may break apart during use and be ejected through the plastic housing, posing a safety hazard to the technician and potentially d
2019-02-06LW Scientific, Inc.The clear, plastic, polycarbonate hematocrit rotor may break apart during use and be ejected through the plastic housing, posing a safety hazard to the technician and potentially d
2017-10-20Terumo BCT, Inc.The patient labels included in the BMAC system procedure packs, catalog numbers 51416 and 51423, are printed with an incorrect lot number, catalog number, and expiry date; the lot
2017-10-20Terumo BCT, Inc.The patient labels included in the BMAC system procedure packs, catalog numbers 51416 and 51423, are printed with an incorrect lot number, catalog number, and expiry date; the lot
2016-02-05Beckman Coulter Inc.A defective rotor yoke on Allegra X-5 allows improper rotor seating on the hub resulting in possible rotor failure if the buckets are loaded in an imbalanced configuration.
2014-12-03Iris DiagnosticsIris International is recalling the RTH8 Rotor used in the StatSpin Express 4 Horizontal Centrifuge because the RTH8 rotor may develop cracks with use over time.
2011-07-15Global Focus Marketing & DevelopPotential for bucket and insert not seated on the rotor to cause the lid to break and buckets to be ejected.
2010-08-18StatSpin, Inc., dba Iris Sample ProcessingRotors may fail due to wire spokes breaking
2010-01-27StatSpin, Inc., dba Iris Sample ProcessingCentrifuge shield micro-switch failed due to damage, and the unit opened, ejecting pieces.

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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.