Instrumentation Laboratory Co. Recalls

Overview of recall records associated with Instrumentation Laboratory Co., including dates, categories and classifications where available.

2recall records

Oct 17, 2018latest record date

Mar 14, 2018earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceOct 17, 2018

Instrumentation Laboratory Co Hemosll ReadiPlasTin (10 mL Size), Part Number 0020301300 recall — FDA Z-0077-2019

There is a potential for increased imprecision, out of range quality controls and prolonged sample results.

Class IIFDA: TerminatedInstrumentation Laboratory Co.

Medical DeviceMar 14, 2018

Instrumentation Laboratory Co Hemosll ReadiPlasTin (20 ml Size), Part Number 0020301400 recall — FDA Z-0895-2018

Instrumentation Laboratory Co. received customer reports of performance issues with some vials of Lot Nos. N1166235 and N0177760, including increased imprecision, out of range quality…

Class IIFDA: TerminatedInstrumentation Laboratory Co.

Understanding this recall history

This page summarizes recall records in which the official source identifies Instrumentation Laboratory Co. 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.