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

Abbott Clinical Chemistry AEROSET c8000 Magnesium, List numbers 7D70-01, 7D70-20, 7D70-30.

FDA Recall Z-0355-04 · Posted 2004-01-16

Recalling FirmAbbott Laboratories Diagnostic Div
Recall StatusTerminated
Product CodeJGJ
Date Initiated2003-12-22
Date Terminated2004-09-21
Product Quantity215

Reason for Recall

Complaints that instructions for use were not clear.

Firm Action

Firm sent customer letters dated 12/22/2003 which included updated instructions for use.

Root Cause

Other

Distribution Pattern

Nationwide and to Mexico, Brazil, Sinagapore, Venezuela, Puerto Rico, Hong Kong, Colombia, Dominican Republic, Australia, Ecuador, Canada, New Zealand, Argentina, Germany, Bahamas, Grand Cayman, El Salvador.

Official Source

View FDA Recall →

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

↑