Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

OLA 2500 Olympus Lab Automation Systems to include the following models (all serial numbers): S2 Full Size, S3 Full Size, Standard Full Size and High Speed Full Size (Aliquoter) manufactured by Olympus Life and Material Science Europa GmbH, Germany and distributed by Olympus America, Inc., 3131 W. Royal Ln., Irving, TX 75063.

FDA Recall Z-0322-06 · Posted 2005-12-23

Recalling FirmOlympus America, Inc
Recall StatusTerminated
Product CodeJQP
Date Initiated2005-11-18
Date Terminated2008-03-10
Product Quantity6 total units.

Reason for Recall

Lab Automation System may dilute samples with water.

Firm Action

Firm initiated recall on 11/18/05 via letter to all direct accounts.

Root Cause

Other

Distribution Pattern

Nationwide; Distribution was made to laboratories and blood centers located in CA, CO, GA, NC, and OH.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑