FDA Enforcement Class II Ongoing

Mechanical Filter with Connector Small, Tethered Cap, Item Code 351/5979 - Product Usage: indicated for single use on anesthetized patients and respiratory care patients who require a breathing circuit with ISO standard 15mm or 22 mm connectors.

Recall: Z-1867-2021 · Reported June 23, 2021

Enforcement

Recall Number
Z-1867-2021
Event ID
87925
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Covidien, LP
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
June 23, 2021
Initiation Date
April 29, 2021
Classification Date
June 16, 2021
Address
60 Middletown Ave, North Haven, CT, 06473-3908, United States

Description

Mechanical Filter with Connector Small, Tethered Cap, Item Code 351/5979 - Product Usage: indicated for single use on anesthetized patients and respiratory care patients who require a breathing circuit with ISO standard 15mm or 22 mm connectors.

Reason

The company was notified by their supplier of sterilization services for airway products in Italy of potential deviations from validated parameters for ethylene oxide sterilization.

Code Info

GTIN Primary Package: 20884522033234 GTIN Secondary Package: 10884522033237 Lot Number: 20J0699FAX

Distribution

Worldwide distribution - US Nationwide distribution in the states of DE, KY, NY, TX, VA, VT, and WA. Global Distribution.

Quantity

7200