FDA recall record

Iotamotion iotaSOFT Plus Drive Unit, REF IM-05 recall — FDA Z-0288-2025

Incorrect GTIN number.

Class IIIclassification
Z-0288-2025official record ID
Nov 13, 2024report date

Recall record at a glance

Official recordZ-0288-2025
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusCompleted
Recalling firmIotamotion Inc.
Report dateNov 13, 2024
Recall initiation dateSep 12, 2024
Quantity5 devices
LocationVadnais Heights, MN, United States

Official product description

iotaSOFT Plus Drive Unit, REF IM-05. The iotaSOFT Insertion System is intended to aid the surgeon in placement of cochlear implant electrode arrays into a radiographically normal cochlea by controlling the speed of implant insertion.

Why the product was recalled

Incorrect GTIN number.

Distribution information

Distribution was made to Iowa. There was no government/military/foreign distribution.

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: Other.

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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