Recently reported

Latest U.S. Recalls

Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.

61,306published records in database
4recall categories represented
Apr 22, 2020newest stored source record
Latest records

Latest recalls — page 1040

The newest recall records with useful source details are listed here.

Medical DeviceApr 22, 2020

Canon Aquilion Premium, Model TSX-301B recall — FDA Z-1721-2020

Scanning may be interrupted due to an error during execution of the eXam Plan and the system is unable to be shut down normally, resulting in the need to forcibly turn the system power off…

Class IIFDA: OngoingCanon Medical System, USA, Inc.
Medical DeviceApr 22, 2020

Canon Aquilion Precision, Model TSX-304A recall — FDA Z-1725-2020

Scanning may be interrupted due to an error during execution of the eXam Plan and the system is unable to be shut down normally, resulting in the need to forcibly turn the system power off…

Class IIFDA: OngoingCanon Medical System, USA, Inc.
Medical DeviceApr 22, 2020

Canon Aquilion Lightning, Model TSX-036A recall — FDA Z-1719-2020

Scanning may be interrupted due to an error during execution of the eXam Plan and the system is unable to be shut down normally, resulting in the need to forcibly turn the system power off…

Class IIFDA: OngoingCanon Medical System, USA, Inc.
Medical DeviceApr 22, 2020

Canon Aquilion Prime, Model TSX-303A recall — FDA Z-1723-2020

Scanning may be interrupted due to an error during execution of the eXam Plan and the system is unable to be shut down normally, resulting in the need to forcibly turn the system power off…

Class IIFDA: OngoingCanon Medical System, USA, Inc.
Medical DeviceApr 22, 2020

Canon Aquilion Prime SP, Model TSX-303B recall — FDA Z-1724-2020

Scanning may be interrupted due to an error during execution of the eXam Plan and the system is unable to be shut down normally, resulting in the need to forcibly turn the system power off…

Class IIFDA: OngoingCanon Medical System, USA, Inc.
Medical DeviceApr 22, 2020

Sysmex The CF-70 instrument recall — FDA Z-1703-2020

Software mismatch-When the software versions between the SP-50 and CF-70 are not matched, and an error condition occurs requiring the operator to open the cover door of the CF-70 to remove…

Class IIFDA: TerminatedSysmex America, Inc.
Browse by month

Recent recall archives

Browse recent months with enough recall history for useful comparison.

Full archive →