The Recall Desk
ModerateFDA (Devices)·Z-0324-2014·Announced 2013-11-27

Ortho-Clinical Diagnostics Recalls VITROS TBIL Slides for Dispense Issues

Ortho-Clinical Diagnostics is recalling VITROS TBIL Slides due to slide dispense issues affecting cartridge functionality.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, and the issue is a mechanical dispense problem rather than a direct biological hazard or reported injury, fitting the criteria for a moderate severity voluntary precautionary recall.

Plain-English summary

Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products TBIL Slides, catalog number 8159931, due to slide dispense issues. These slides are used to quantitatively measure total bilirubin concentration in serum and plasma on VITROS Chemistry Systems.

The recall involves 175,689 units, with 86,745 units distributed domestically in the United States and 88,944 units distributed internationally. The affected lots have expiry dates through March 22, 2015.

Healthcare facilities and users of the affected VITROS systems should stop using the recalled slides and contact Ortho-Clinical Diagnostics for further instructions.

The recalled product

Product
VITROS Chemistry Products TBIL Slides packaged as 300 slides/pack catalog number 8159931 VITROS TBIL Slides quantitatively measure total bilirubin (TBIL) concentration in serum and plasma using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the VITROS 5600 Integrated S

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • Multiple lots affected
  • with expiry dates through 22-Mar-2015

Distribution

Distributed nationwide across the United States.

The notice also names 50 states specifically:

Part of a larger recall action

This product is one of 37 recalled by Ortho-Clinical Diagnostics under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 37 products in this recall →