Instrumentation Laboratory Co.: Medical Device Recall in 2018 - (Recall #: Z-0895-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Hemosll ReadiPlasTin (20 ml Size), Part Number 0020301400

Product Classification:

Class II

Date Initiated: August 2, 2017

Date Posted: March 14, 2018

Recall Number: Z-0895-2018

Event ID: 79165

Reason for Recall:

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 controls and prolonged sample results.

Status: Terminated

Product Quantity: 14,894 kits

Code Information:

Lots: N1166235, N0177760, N0278358, N0478057, N0479504 & N0278177.

Distribution Pattern:

Worldwide Distribution - US Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated