Sterling Diagnostics, Inc. recalls Sterling Diagnostics, Inc., HDL Cholesterol (PEF Method) for IN VITRO DIAGNOSTIC USE in the quantitative determination o

Recalled January 4, 2017 · FDA recall Z-0930-2017 · Sterling Diagnostics

Hazard

Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple diagnostic kits due to a recision of the previously extended expiration dates for the kits. · FDA Class III

Units

245

Sold at

Domestic: MI Foreign: Phillipines VA/DOD: None

Description

Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple diagnostic kits due to a recision of the previously extended expiration dates for the kits.

Product

Sterling Diagnostics, Inc., HDL Cholesterol (PEF Method) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a customer buys another when kit is consumed.

Manufacturer(s)

Sterling Diagnostics, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →