FDA Device Intelligence
HomeSTRECK, INC. › ESR-Auto Plus

ESR-Auto Plus

STRECK, INC. · Model 506 · UDI-DI 00844509002147

GKB
2
510(k) clearances
5
Adverse events
3
Recalls
17
Facilities

Description

A 10-position automated sed-rate analyzer.

Recalls

DateFirmReason
2023-04-14Mechatronics USAQRR049001 Lot QCAB6AN505 incorrectly labelled as QRR049002 Lot QCAB6AAA28. The incorrectly labelled vial will upload the range for the Starrsed Control Level A and the instrument r
2023-04-14Mechatronics USAQRR049001 Lot QCAB6AN505 incorrectly labelled as QRR049002 Lot QCAB6AAA28. The incorrectly labelled vial will upload the range for the Starrsed Control Level A and the instrument r
2022-07-20Alcor Scientific, Inc.Primary Pump Tubing Spare Part is incorrect. If the tubing is installed onto an ALCOR iSED ESR Analyzer, there is a potential of a biohazard leak from the iSEDs Probe Tube

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.