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Diagnostic Hybrids Inc Recalls

7 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Diagnostic Hybrids Inc.

7Total Recalls
0Critical
14,486Units Affected
Apr 4, 2017Most Recent
All Recalls

Every Diagnostic Hybrids Inc Recall

Sorted by most recent. Click any recall for full details.

7 recalls
High RiskFDA
Diagnostic Hybrids, Inc.
MicroVue CIC-C1q EIA, Model A001. An enzyme immunoassay for the detection of circulating immune complexes in human serum or plasma. The...
Diagnostic Devices·101 affected·Apr 4, 2017
RecallFDA
Diagnostic Hybrids, Inc.
Quidel MicroVue Intact PTH EIA, Model 8044. An enzyme immunoassay for the quantification of Intact Parathyroid Hormone (PTH) in serum.
Diagnostic Devices·26 affected·Oct 26, 2016
High RiskFDA
Diagnostic Hybrids, Inc.
MicroVue BAP EIA, Model 8012, provides a quantitative measure of bone-specific alkaline phosphatase (BAP) activity in serum.
Medical Devices·1,004 affected·Jul 14, 2016
RecallFDA
Diagnostic Hybrids, Inc.
MicroVue SC5b-9 Plus EIA (CE-IVD), Model A029. An enzyme immunoassay for the quantitation of SC5b-9 complex present in human plasma or s...
Diagnostic Devices·72 affected·Nov 3, 2015
RecallFDA
Diagnostic Hybrids, Inc.
MicroVue SC5b-9 Plus EIA (RUO), Model A020. Research use only (RUO) product. An enzyme immunoassay for the quantitation of SC5b-9 comple...
Diagnostic Devices·107 affected·Nov 3, 2015
High RiskFDA
Diagnostic Hybrids Inc
MicroVue Bb Plus EIA is packaged as a kit which contains all reagent components to perform the test. In vitro diagnostic.
Diagnostic Devices·171 affected·Oct 16, 2014
RecallFDA
Diagnostic Hybrids Inc
Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture media, used in the cultivation and amplificat...
Respiratory Devices·13,005 affected·Dec 31, 2012