Every recall we track for Philips Medical Systems Gmbh, DMC — 33 in all — plus the complaints and injury reports the public filed about them.
Philips recalls CombiDiagnost R90 software versions R1.0 and R1.1 due to potential image exposure issues. Affected units may produce over or under exposed images.
Philips recalls CombiDiagnost PCF software v1.0.5 for error 80 locking geometry and incorrect thermos switch installation. Affected units may require service engineer intervention.
Philips recalls CombiDiagnost GCF software v1.0.5 (Product Code 709030) for error 80 locking geometry and incorrect thermos switch installation. Affected units may require service engineer intervention.
Philips recalls CombiDiagnost R90 X-ray systems with software versions 1.0.0-1.0.2 due to potential increased radiation exposure during patient scans. Affected units may require software update or repair.
Philips recalls X-ray software versions 4.1.x and 4.2.x for stationary systems with serial numbers starting 547772 to SN18000227. The software has stitching errors that may cause system interruptions during imaging.
Philips recalls DigitalDiagnost Rel.4 Upgrades (Stitching Patient Support) 712084 due to footplate safety risk. Affected units have serial numbers SN15000153, SN17000147, SN15000211, SN17000160.
Philips recalls DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031 with serial numbers listed. The footplate may fall or swing down, risking injury to operator or patient. Affected units must be checked and addressed.
Philips recalls DigitalDiagnost 712052 models with footplate that may fall or swing, risking operator or patient injury. Affected units have specific serial numbers.
Philips recalls DigitalDiagnost 4 Flex Stitching Patient Support models with serial numbers SN17000283 and others due to risk of footplate falling and injuring operator or patient during use.
Philips recalls DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 with serial numbers listed. The footplate may fall or swing down, risking injury to operator or patient. Stop using immediately.
Philips recalls DigitalDiagnost Classic Dual-Detector models with stitching patient support due to footplate falling risk. Affected units have specific serial numbers. Stop using immediately to prevent injury.
Philips recalls CombiDiagnost R90 Stitching Patient Support model 709030 due to risk of footplate falling and causing injury during use. Affected units have specific serial numbers.
Philips recalls DigitalDiagnost Classic 1.x Upgrades (Stitching Patient Support) 712081 due to footplate that may fall or swing, risking operator or patient injury. Affected units have specific serial numbers.
Philips recalls DigitalDiagnost 4.1 Stitching Patient Support model 712225 due to risk of footplate falling and injuring operator or patient. Affected units have serial number SN16000137.
Philips recalls EasyDiagnost Eleva DRF Release 5 (Stitching Patient Support) 706050 due to risk of footplate falling and injuring operator or patient. Affected units have specific serial numbers listed in the recall notice.
Philips recalls DigitalDiagnost 4 Chest/Emergency Stitching Patient Support model 712029 due to footplate safety risk. Affected units may cause injury if footplate falls or swings down during use.
Philips Medical Systems recalls DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026 due to risk of footplate falling and causing injury during use. Affected units have specific serial numbers listed in the recall.
Philips recalls DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712082 due to footplate falling or swinging, potentially injuring operator or patient. Affected units have specific serial numbers.
Philips recalls DigitalDiagnost Stitching Patient Support model 712062 due to footplate falling risk. Affected units have specific serial numbers. Stop using immediately to prevent injury.
Philips recalls DigitalDiagnost 4.1 Chest/Emergency (Stitching Patient Support) 712029 due to footplate falling risk. Affected units have serial number SN15000433. Stop using immediately to prevent injury.
Philips Medical Systems recalls DigitalDiagnost Upgrades (Stitching Patient Support) 712083 due to footplate not securely holding position, risking injury to operator or patient. Affected units have specific serial numbers listed.
Philips recalls DigitalDiagnost Release 3 Stitching Patient Support models with serial numbers 510694/SN12000240 to 511346/SN13000008. The footplate may fall or swing, risking injury to operator or patient.
Philips recalls DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081 due to footplate safety risk. Affected units may cause injury if footplate falls or swings down during use.
Philips Medical recalls DigitalDiagnost Release 3 Stitching Patient Support models with serial numbers starting 492928-519609. The footplate may fall, causing injury to operator or patient. Stop using immediately.
Philips recalls DigitalDiagnost 4 High Performance (Stitching Patient Support) 712027 with serial numbers listed. The footplate may fall or swing down, risking injury to operator or patient.
Philips Medical recalls DigitalDiagnost 4.1 Flex patient support units with serial numbers starting with SN15000 or SN16000. The footplate may fall or swing down, risking injury to operator or patient.
Philips Medical Systems recalls DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026 due to footplate falling risk. Affected units have specific serial numbers listed in the recall notice.
Philips recalls DigitalDiagnost 4 Flex patient support units with serial numbers SN17000395 and SN17000372 due to risk of footplate falling and causing injury during use.
Philips recalls EasyDiagnost Eleva DRF Stitching Patient Support model 706032 due to risk of footplate falling and causing injury. Affected units have specific serial numbers listed in the recall notice.
Philips recalls DigitalDiagnost Single Detector (Stitching Patient Support) 712020 due to footplate instability. This could cause injury to operator or patient if the footplate falls or swings down.
Philips recalls DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031 with serial numbers SN15000196, SN15000180, SN15000282, SN15000281, SN15000192, and SN15000189 due to risk of footplate falling and causing injury to operator or patient.
Philips recalls DigitalDiagnost Dual Detector (Stitching Patient Support) model 712022 due to footplate instability that could cause injury to operator or patient. Affected units have specific serial numbers listed.
Philips recalls BuckyDiagnost Ceiling System (Stitching Patient Support) 704031 due to footplate falling risk. Affected units have serial numbers starting with 477195/SN110: stop using immediately.
