Sterling Diagnostics Recalls Enzymatic Glucose Diagnostic Kits
Sterling Diagnostics is recalling 40 units of Enzymatic Glucose diagnostic kits due to a revision of previously extended expiration dates.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is classified as FDA Class III, which is defined as unlikely to cause adverse health consequences. The issue is a documentation/labeling correction regarding expiration dates rather than a physical defect or contamination.
Plain-English summary
Sterling Diagnostics, Inc. initiated a recall on July 20, 2016, for 40 units of Enzymatic Glucose diagnostic kits. These products are intended for in vitro diagnostic use in the quantitative determination of analytes and are classified as consumables.
The recall was initiated due to a revision of the previously extended expiration dates for the kits. The specific product details include Catalog No. 2185-L, Lot No. 18561, with an expiration date of May 2019 and a manufacture date of May 25, 2016.
The affected units were distributed domestically in Michigan and internationally to the Philippines. No distribution to VA/DOD facilities is reported. Users should stop using the affected kits and contact Sterling Diagnostics for further instructions.
The recalled product
- Product
- 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.
- Manufacturer
- Sterling Diagnostics, Inc.
- Hazard
- Affected units
- 40
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 (5)
- Enzymatic Glucose
- CAT No. 2185-L
- Lot No. 18561
- Expriry: 5/19
- Manufactured: 05/25/16
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 9 recalled by Sterling Diagnostics, Inc. 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.
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