Home › Companies › Konica Minolta Medical Imaging USA, Inc.

Recall company profile

Konica Minolta Medical Imaging USA, Inc. Recalls

Overview of recall records associated with Konica Minolta Medical Imaging USA, Inc., including dates, categories and classifications where available.

6recall records

Jul 4, 2018latest record date

Apr 4, 2018earliest record date

Recall history in this database

Classification mix: Class II: 6.

Medical DeviceJul 4, 2018

Konica Minolta Medical Imaging USA CS-7, Model No. A4C1 recall — FDA Z-2281-2018

Panasonic has issued a Mandatory Product Safety Notice, indicating a possibility of battery ignition (fire) in CF-C2 "Toughbook" laptops. Since Konica Minolta uses this laptop in some of…

Class IIFDA: TerminatedKonica Minolta Medical Imaging USA, Inc.

Medical DeviceJul 4, 2018

Konica Minolta Medical Imaging USA ImagePilot, Model No recall — FDA Z-2282-2018

Panasonic has issued a Mandatory Product Safety Notice, indicating a possibility of battery ignition (fire) in CF-C2 "Toughbook" laptops. Since Konica Minolta uses this laptop in some of…

Class IIFDA: TerminatedKonica Minolta Medical Imaging USA, Inc.

Medical DeviceApr 4, 2018

Konica Minolta Medical Imaging USA Sonimage HS1 Ultrasound Kit AC adapter, Product Number recall — FDA Z-1215-2018

There is a risk of circuit board breakage within the main housing of the AC Adapter unit. Smoke may be emitted from the AC Adapter as a direct result.

Class IIFDA: TerminatedKonica Minolta Medical Imaging USA, Inc.

Medical DeviceApr 4, 2018

Konica Minolta Medical Imaging USA Sonimage HS1 Ultrasound Kit AC adapter, Product Number: 1 recall — FDA Z-1214-2018

There is a risk of circuit board breakage within the main housing of the AC Adapter unit. Smoke may be emitted from the AC Adapter as a direct result.

Class IIFDA: TerminatedKonica Minolta Medical Imaging USA, Inc.

Medical DeviceApr 4, 2018

Konica Minolta Medical Imaging USA Sonimage HS1 Ultrasound Kit AC adapter, Product Number recall — FDA Z-1213-2018

There is a risk of circuit board breakage within the main housing of the AC Adapter unit. Smoke may be emitted from the AC Adapter as a direct result.

Class IIFDA: TerminatedKonica Minolta Medical Imaging USA, Inc.

Medical DeviceApr 4, 2018

Konica Minolta Medical Imaging USA Sonimage HS1 Ultrasound Kit AC adapter, Product Number recall — FDA Z-1212-2018

There is a risk of circuit board breakage within the main housing of the AC Adapter unit. Smoke may be emitted from the AC Adapter as a direct result.

Class IIFDA: TerminatedKonica Minolta Medical Imaging USA, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Konica Minolta Medical Imaging USA, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.