United StatesBeckman Coulter Access 2 Reaction Vessels (individual disposable plastic tubes for the Access 2 Immunoassay system, Catalog Number 81901; UDI-DI 15099590180249) from lot numbers P243943, P243971, P244202, P244344, P244345, P250001–P250005 are affected. Certain lots may have a small protrusion or hair-like deformity on the bottom end that can cause instrument errors (for example pipetting, rake or wash carousel errors) and could delay patient results.
What's being recalled
Access 2 Reaction Vessels, individual, disposable, plastic tubes used to process patient, quality control and calibration samples on the Access 2 Immunoassay system, Catalog Number 81901
Recalling firm: Beckman Coulter, Inc., Chaska, MN, United States.
How to identify it
UDI-DI: 15099590180249; Lot Numbers: P243943, P243971, P244202 P244344, P244345, P250001, P250002, P250003, P250004 and P250005
The hazard
It has been determined that certain lots of Access 2 Reaction Vessels may contain manufacturing deformities. The bottom (round end) of the Reaction Vessel may have a small protrusion or hair like deformity. This could cause causing instrument errors (e.g., pipetting, rake, wash carousel errors) that could delay patient results.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide. Global Distribution.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)
Canada