FDA recall record

bioMerieux eMAG System, Ref 418591 It is an In Vitro Diagnostic Medical device intended for recall — FDA Z-3119-2017

Some anomalies have been identified during manufacturing controls.

Class IIclassification
Z-3119-2017official record ID
Sep 20, 2017report date

Recall record at a glance

Official recordZ-3119-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmbioMerieux, Inc.
Report dateSep 20, 2017
Recall initiation dateApr 10, 2017
Quantity15 US
LocationDurham, NC, United States

Official product description

eMAG System, Ref 418591 It is an In Vitro Diagnostic Medical device intended for the automated isolation (purification and concentration) of total nucleic acids (RNA/DNA) from biological specimens, with liquid and homogeneous properties (as part of their natural characteristics or after pre-treatment).

Why the product was recalled

Some anomalies have been identified during manufacturing controls.

Distribution information

Worldwide Distribution: US (nationwide) to states of: GA, IL, IN, MA, NC & TX and to countries of: Austria, France, Germany, Hong Kong, Italy, Netherlands, Spain, Sweden, Switzerland, Thailand and United Kingdom.

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: 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.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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