FDA Recall Open, Classified

NORMOFLO Irrigation Fluid Warmer Models H-1100 and H-1129

Recall: Z-2376-2021 · Initiated August 6, 2021

Recall

Recall Number
Z-2376-2021
Event Number
88455
Firm
Smiths Medical ASD Inc.
FEI Number
3012307300
Product Code
LGZ
Status
Open, Classified
Root Cause
Device Design
Initiated
August 6, 2021
Address
6000 Nathan Ln N, Minneapolis, MN, 55442-1690

Description

NORMOFLO Irrigation Fluid Warmer Models H-1100 and H-1129

Reason

There is potential for harmful levels of aluminum leaching when using lower flow rates with certain solutions and blood products and longer duration of use.

Action

Smiths Medical sent an Urgent Medical Device Recall Notice and attachments dated August 13, 2021 to all affected customers. The letter instructed all customers who purchased affected devices listed in the table on page 1 of the Urgent Medical Device Recall Notice must identify any of the affected products within their possession and refer to the detailed instructions on pages 2 and 3 of the notice. Distributors will be instructed to immediately forward a copy of the Urgent Medical Device Recall Notice and attachments to any customers to whom they have distributed affected product. Distributors will also be instructed to request that customers to who they have distributed affected product complete the Response Form and return it to the distributor. Distributors will indicate their identity as the distributor and document the consignees name and address. Questions regarding this recall notification may be forwarded to [email protected].

Distribution

US Nationwide Distribution and PR OUS distribution in - Austria, Australia, Belgium, Switzerland, Canada, Germany, Spain, Finland, France, United Kingdom, Greece, Hong Kong, Hungary, Ireland, Italy, Kuwait, Luxembourg, Netherlands, New Zealand, Panama, Poland, Portugal, Sweden, Turkey, Venezuela, South Africa

Quantity

913