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Helena Laboratories, Corp. recalls V8 Immunodisplacement Kit REF 1803
Recalled June 15, 2022 · FDA recall Z-1244-2022 · Helena Laboratories
Hazard
Due to microbial growth causing interference with interpretation. · FDA Class II
Units
51 kits
Sold at
U.S.: FL, MO, OH, and TX O.U.S.: Canada, Uruguay, and Vietnam,
Description
Due to microbial growth causing interference with interpretation.
Product
V8 Immunodisplacement Kit REF 1803
Manufacturer(s)
Helena Laboratories, Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →