Konica Minolta Medical Imaging USA, Inc. Regius Model 370 Digital Radiography Konica Minolta Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Regius Model 370 Digital Radiography Konica Minolta
Brand
Konica Minolta Medical Imaging USA, Inc.
Lot Codes / Batch Numbers
Serial # 0729-0005
Products Sold
Serial # 0729-0005
Konica Minolta Medical Imaging USA, Inc. is recalling Regius Model 370 Digital Radiography Konica Minolta due to A hand grip column, even though locked in position, moved downward about 3 cm while a patient was holding the hand grip for lateral exposure. When th. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
A hand grip column, even though locked in position, moved downward about 3 cm while a patient was holding the hand grip for lateral exposure. When the hand grip moved down, the patient who was holding it lost his or her balance and almost fell. This problem only occurred in Japan with one system.
Recommended Action
Per FDA guidance
Konica Minolta USA contacted the site of the sole US user by phone on 7/14/06, followed by e-mail and certified mail/return receipt.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
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Page updated: Jan 10, 2026