FDA Recall Terminated

First Breath Adult Face Tent with Tubing 188cm (5ft.) (Non-latex) Reorder Number: 001492 Face Tent Is a special type of aerosol mask used when the delivery of oxygen is not the primary objective. Normally this type of mask is used to deliver an aerosol mist to cool and moisturize the nasal passages or sinuses after surgery

Recall: Z-2654-2011 · Initiated February 11, 2011

Recall

Recall Number
Z-2654-2011
Event Number
57906
Firm
Smiths Medical Hythe Hythe, Kent United Kingdom
FEI Number
3002807908
Product Code
BYG
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
February 11, 2011
Posted
June 24, 2011
Terminated
July 2, 2018

Description

First Breath Adult Face Tent with Tubing 188cm (5ft.) (Non-latex) Reorder Number: 001492 Face Tent Is a special type of aerosol mask used when the delivery of oxygen is not the primary objective. Normally this type of mask is used to deliver an aerosol mist to cool and moisturize the nasal passages or sinuses after surgery

Reason

A sticky substance on the inside and/ or outside of the Mask

Action

Smiths Medical notified consignees by letter on 2/14/11 titled Urgent Medical Device Correction Notice via U.S. Mail (USA only) This Notice includes an Urgent Medical Device Correction Notice Confirmation Form that provides instructions to consignees to return unused affected product to Smiths Medical and to complete the effectivity tracking form. On 3/17/11 Smiths Medical issued an additional recall letter to extend the recall to 3 additional lots not included in the original recall letter dated 2/14/11. Also, the firm issued a recall letter on 3/17/11 to include the Value Pack (VP1302) General Anesthesia Kit to include 7 kit lots. Contact Recall Coordinator 1-800-348-6064 prompt 4, ext 2273

Distribution

Worldwide Distribution - USA (nationwide) and the countries of United Arab Emirates, Armenia, Brazil, Canada, France, Hungary, Italy, Jordan, Japan, Libya, Poland, Russian Federation, and Saudi Arabia.

Quantity

600 units