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

Circuit-Unilimb, Adult, 1M (40''), Disposable, Clean Non-sterile, Adult Anesthesia Circuit, Part Numbers DYNJAAF4000, DYNJAAF6225, and DYNJAAF6261. Manufactured for Medline Industries, Inc., Mundelein, IL 60060, Made in Mexico.

FDA Recall Z-0768-05 · Posted 2005-04-27

Recalling FirmMMS Sales Corp
Recall StatusTerminated
Product CodeCAI
Date Initiated2005-02-21
Date Terminated2006-12-20
Product QuantityTotal for all products: 7455 cases (161,273 units)

Reason for Recall

Partial occlusion in the T-piece resulting in airway obstruction.

Firm Action

The firm initiated the recall on February 21, 2004 by letter to all consignees.

Root Cause

Other

Distribution Pattern

Product was distributed domestically to customers in CA, AZ, IL, CO, OR, FL, VA, OH, MI, and UT. Product was also distributed to the following foreign countries: Malaysia, Mexico, and New Zealand

Official Source

View FDA Recall →

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

↑