FDA recall record

Inpeco S.A FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2), Laboratory recall — FDA Z-1798-2018

Module may freeze without generating user warning. There is a potential risk in delay of sample processing, leading to delayed delivery of test results to…

Class IIclassification
Z-1798-2018official record ID
May 16, 2018report date

Recall record at a glance

Official recordZ-1798-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmInpeco S.A.
Report dateMay 16, 2018
Recall initiation dateFeb 13, 2018
Quantity18
LocationLugano, N/A, Switzerland

Official product description

FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2), Laboratory Automation System

Why the product was recalled

Module may freeze without generating user warning. There is a potential risk in delay of sample processing, leading to delayed delivery of test results to patients.

Distribution information

Distributors in 2 states: NY and IL.

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.

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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