International safety notice
Common name: General purpose ultrasound imaging device Brand name: Ultrasound imaging device EPIQ/Affiniti
Japan / PMDA Recalls · JPN · Nov 4, 2021
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | Common name: General purpose ultrasound imaging device Brand name: Ultrasound imaging device EPIQ/Affiniti |
| Manufacturer | Philips Japan Co., Ltd. |
| Models | USO15B0925，USO15B0926，USO15B1124，USO15B1205，USO16B0123，USO16B0673，USO16F0089，USO17C0049，, US220F1485，US315B0034，US315B0126，US315B1059，US315B1190，US316B0220，US317B0083，US318B2536，, USO18B0277，USO19B0696，USO19B0697，USO19B2711，USO19C1874，USO19D0047，USO19E0648，USO19F1038，, USN17B0906，USN17B1689，USN17C0968，USN18B1321，USN18B1417，USN18D1294，USN18F0144，USN18F2251，, US819F1364，US819F1746，US914F0582，US914F0879，US915B0860，US915B0867，US915B1055，US915F0888，, US216D0339，US217B0314，US217C0096，US218B0504，US219B1173，US219B1174，US219B1312，US219E0226，, US120B1445，US120B1551，US120B1554，US120B1556，US120B1764，US120B1876，US120C0407，US120D0379，, USD19B1137，USD19D0331，USD19D0724，USD19E0388，USD19E0389，USD19E0873，USD19F0077，USD19F0171，, US120B0239，US120B0394，US120B0399，US120B0400，US120B0939，US120B1036，US120B1116，US120B1117，, USD15D0790，USD16B1201，USD16B1291，USD19B0239，USD19B0306，USD19B0623，USD19B0965，USD19B1090，, US917B1601，US917C1668，US918B1643，US918B1775，US919B0351，US919B0476，US919B0486，US919B0712，, US220B0374，US220B0414，US220B0523，US220B0557，US220B0665，US220B0706，US220B0863，US220B1124， and 24 more |
| Date | Nov 4, 2021 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1