NeoCoil, LLC Recalls

Overview of recall records associated with NeoCoil, LLC, including dates, categories and classifications where available.

2recall records

Aug 10, 2016latest record date

Mar 9, 2016earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceAug 10, 2016

NeoCoil 3T 16ch Flex SPEEDER Coil, Large, NeoCoil Part Number NC046200, Toshiba Medical recall — FDA Z-2312-2016

There is a potential for higher than specified surface temperatures involving the 3T 16ch Flex SPEEDER Large Coil.

Class IIFDA: TerminatedNeoCoil, LLC

Medical DeviceMar 9, 2016

NeoCoil 3.0T GEM Flex Coil recall — FDA Z-1027-2016

Potential for higher than specified surface temperatures. Use of 3.0T GEM Flex system may result in patient warming or burns.

Class IIFDA: TerminatedNeoCoil, LLC

Understanding this recall history

This page summarizes recall records in which the official source identifies NeoCoil, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.