FDA recall record

Helena Laboratories Titan Gel Serum Protein Control: SPE Control Cat recall — FDA Z-2434-2019

Due to customer-experienced complaints on narrow assay range compared to prior lots and the user being out of assay range.

Class IIclassification
Z-2434-2019official record ID
Sep 11, 2019report date

Recall record at a glance

Official recordZ-2434-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmHelena Laboratories, Inc.
Report dateSep 11, 2019
Recall initiation dateOct 14, 2016
Quantity65 kits
LocationBeaumont, TX, United States

Official product description

Titan Gel Serum Protein Control: SPE Control Cat. No 5136 1 x 2.0 mL

Why the product was recalled

Due to customer-experienced complaints on narrow assay range compared to prior lots and the user being out of assay range.

Distribution information

Domestic: FL, IL, MN, MT, NY, OH, TN, TX, VA, and WI OUS: Australia, Canada, Jordan, and South Korea

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

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

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

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