FDA recall record

Tosoh Bioscience AIA-PACK TgAb CONTROL SET recall — FDA Z-2169-2017

The label contains two different methodologies. Quality Control values for non-FDA approved methodology (CL) are on the label in addition to the FDA…

Class IIIclassification
Z-2169-2017official record ID
Jun 7, 2017report date

Recall record at a glance

Official recordZ-2169-2017
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmTosoh Bioscience, Inc.
Report dateJun 7, 2017
Recall initiation dateFeb 8, 2017
Quantity64 boxes
LocationSouth San Francisco, CA, United States

Official product description

AIA-PACK TgAb CONTROL SET

Why the product was recalled

The label contains two different methodologies. Quality Control values for non-FDA approved methodology (CL) are on the label in addition to the FDA approved methodology values (AIA). Two sets of instructions were included on the label.

Distribution information

Product was shipped to the following states: AK, FL, GA, MA, NY, NY, OH, OK & TX.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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