FDA recall record

Wiener Lab CHAGATEST ELISA RECOMBINANTE V. 3.0 Diagnosis of Chagas disease recall — FDA Z-0924-2018

Internal program testing shows that product may not reach the indicated expiration date.

Class IIclassification
Z-0924-2018official record ID
Mar 14, 2018report date

Recall record at a glance

Official recordZ-0924-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmWiener Laboratories
Report dateMar 14, 2018
Recall initiation dateNov 10, 2017
Quantity1,563 units
LocationRiobamba, N/A, Argentina

Official product description

Wiener Lab CHAGATEST ELISA RECOMBINANTE V. 3.0 Diagnosis of Chagas disease.

Why the product was recalled

Internal program testing shows that product may not reach the indicated expiration date.

Distribution information

Worldwide Distribution - US Distribution to the states of : Florida and Washington DC. , and to the countries of : Argentina, Bolivia, Brasil, and Costa Rica.

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: E-Mail.

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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