Barbiturates Intercept Micro-Plate EIA (enzyme immunoassay, barbiturate) Product is intended for use by clinical laboratories in the qualitative determination of barbiturates in oral fluids.
Reported: December 14, 2016 Initiated: November 10, 2016 #Z-0722-2017
Product Description
Barbiturates Intercept Micro-Plate EIA (enzyme immunoassay, barbiturate) Product is intended for use by clinical laboratories in the qualitative determination of barbiturates in oral fluids.
Reason for Recall
Shipping error. Cocaine metabolite Microplate distributed instead of Barbiturate Microplate due to incorrect selection of Microplate during manufacturing.
Details
- Recalling Firm
- OraSure Technologies, Inc.
- Units Affected
- 4 kits
- Distribution
- Distributed to KS, and VA
- Location
- Bethlehem, PA
Frequently Asked Questions
What product was recalled? ▼
Barbiturates Intercept Micro-Plate EIA (enzyme immunoassay, barbiturate) Product is intended for use by clinical laboratories in the qualitative determination of barbiturates in oral fluids.. Recalled by OraSure Technologies, Inc.. Units affected: 4 kits.
Why was this product recalled? ▼
Shipping error. Cocaine metabolite Microplate distributed instead of Barbiturate Microplate due to incorrect selection of Microplate during manufacturing.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 14, 2016. Severity: Low. Recall number: Z-0722-2017.
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