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

Kendall Curity Disposable Laparotomy Sponges, 12 in x 12 in, Sterile Product Number: 6034

FDA Recall Z-0382-04 · Posted 2004-07-20

Recalling FirmKendall Healthcare Products Co
Recall StatusTerminated
Product CodeNAD
Date Initiated2004-01-08
Date Terminated2012-05-15
Product Quantity188 cases

Reason for Recall

Sterility compromised due to lack of package seal integrity

Firm Action

Kendall issued Recall letters by US Mail to all customers on January 8, 2004, requesting product be returne and dealer customers be notified.

Root Cause

Other

Distribution Pattern

AL, AZ, CA, CO, FL, GA, IL, KY, LA, MA, MD, MN, MO,NC NE, NJ, NY, OH, PA, RI, TN, TX, VA, WA, WI, WV.

Official Source

View FDA Recall →

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

↑