medical Class II Updated 2022-06-15

Helena Laboratories, Corp. recalls V8 Immunodisplacement Kit REF 1803

Recalled Product

V8 Immunodisplacement Kit REF 1803

Hazard / Issue

Due to microbial growth causing interference with interpretation.

Issued by

FDA

Affected States: FL, MO, OH, TX
Lot/Code Info: Model Number: 1803 UDI Codes: +M52518030/SS73-21-1803/14D20230831Z +M52518030/SS71-21-1803/14D20230830X Lot 3-21-1803 Lot 1-22-1803
View official government recall

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