Medical device recalls

Sterling Diagnostics, Inc. recalls Sterling Diagnostics, Inc., Enzymatic Glucose for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes…

Recall date
July 20, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0932-2017
FDA classification
Class III
Brand / firm
Sterling Diagnostics, Inc.
Sold / distributed
Domestic: MI Foreign: Phillipines VA/DOD: None

Why it was recalled

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.

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

Sterling Diagnostics, Inc., Enzymatic Glucose for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a customer buys another when kit is consumed.

Get recall alerts

Free email alert whenever Sterling Diagnostics, Inc. has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Sterling Diagnostics, Inc.