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FDA (Device enforcement)Recalled 2025-07-03class iii

Philips Ultrasound, Inc: L12-5 50 Transducer Probe

Hazard

To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

Details from the source

Reason for recall: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. Distribution: US Nationwide distribution. Quantity: 171,322 units Lot/code info: Model No. 989605418552, 989605408173, 989605438481, 989605420231, 989605412401, 989605408171, 989605362313, 989605396002, 989605387311, 989605412042, 989605418551, 989605409562, 989605412072, 989605409582, 989605440931, 989605361882, 989605440932; UDI: (01)00884838067851(21)B1N28J, (01)00884838067851(21)B1N2GB, (01)00884838067851(21)B20JW8, (01)00884838067851(21)B2TL6N, (01)00884838067851(21)B2TM54, (01)00884838067851(21)B2TNPZ, (01)00884838067851(21)B2TPD0, (01)00884838067851(21)B2ZJYP, (01)00884838067974(21)B24F91, (01)00884838067851(21)B2TMH2, 010088483806785121F0FNVH, 010088483806785121F0FQMW, 010088483806785121F0FQNJ, (01)00884838067851(21)B24NM7, (01)00884838067851(21)B2D9MB, (01)00884838067851(21)B2D9VH, (01)00884838067851(21)B2H8B5, (01)00884838067851(21)B2PL21, (01)00884838067851(21)B40HY0, (01)00884838067851(21)B40J43, (01)00884838067974(21)B1N1NV, (01)00884838067851(21)B3XX7R, (01)00884838067851(21)F088MN, (01)00884838067851(21)B0P7DV, (01)00884838067851(21)B2ZHQ3, (01)00884838067851(21)B40VT9, (01)00884838067851(21)F0589C, (01)00884838067851(21)F0CHBM, (01)00884838067851(21)F0FNT5, (01)00884838067851(21)F0JZNN, 010088483806785121F0FZWN, 010088483806785121F0FZXK, (01)00884838067851(21)B20QHY, (01)00884838067851(21)B20GD4, (01)00884838067851(21)F0JTMB, 010088483806785121B3XJNR, (01)00884838067851(21)B39N0H, (01)00884838067974(21)B0LMXB, (01)00884838067974(21)B2H5LC, (01)00884838067974(21)B2PR9K, (01)00884838067974(21)B2ZK20, (01)00884838067974(21)B2ZW1C, (01)0088483

UPC codes

989605418552, 989605408173, 989605438481, 989605420231, 989605412401, 989605408171, 989605362313, 989605396002, 989605387311, 989605412042, 989605418551, 989605409562, 989605412072, 989605409582, 989605440931, 989605361882, 989605440932, 00884838067851, 00884838067974, 00884838064560, 00884838061569, 00884838061613

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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