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Aniara Diagnostica Llc Recalls

6 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Aniara Diagnostica Llc.

6Total Recalls
0Critical
124Units Affected
Feb 1, 2023Most Recent
All Recalls

Every Aniara Diagnostica Llc Recall

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

6 recalls
High RiskFDA
Aniara Diagnostica Llc
BIOPHEN Protein C 5 kit is for in vitro quantitative determination of Protein C activity on human citrated plasma. Protein C is a glycopr...
Medical Devices·2 affected·Feb 1, 2023
RecallFDA
Aniara Diagnostica Llc
BIOPHEN UFH Control Plasma
Medical Devices·13 affected·Jun 28, 2022
High RiskFDA
Aniara Diagnostica Llc
ZYMUTEST HIA MonoStrip, IgG ELISA kit, Model No. RK041A, for in vitro diagnostic use.
Diagnostic Devices·51 affected·Jul 19, 2019
RecallFDA
Aniara Diagnostica Llc
BIOPHEN UFH Control C1, REF 224101
Medical Devices·41 affected·Mar 19, 2019
RecallFDA
Aniara Diagnostica Llc
BIOPHEN LMWH Control C4, REF 224201
Medical Devices·3 affected·Mar 19, 2019
RecallFDA
Aniara Diagnostica Llc
BIOPHEN UFH Control C2, REF 223901
Medical Devices·14 affected·Mar 19, 2019