medical Class III Updated 2017-01-04

Sterling Diagnostics, Inc. recalls Creatinine/Endpoint [Modified Heinegard-Tiderstrom] for IN V

Recalled Product

Creatinine/Endpoint [Modified Heinegard-Tiderstrom] for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a customer buys another when kit is consumed.

Hazard / Issue

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.

Issued by

FDA

Affected States: MI, VA
Lot/Code Info: Creatinine/Endpoint [Modified Heinegard-Tiderstrom], CAT No. 2167-O, Lot No. 16751, Expriry: 5/18, Manufactured: 06/02/15
View official government recall

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