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

Philips Ultrasound, Inc: L12-4 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. 989605430652, 989605409562, 989605427122, 989605463401, 989605430651, 989605442161, 989605418963, 989605387852, 989605418701, 989605387081, 989605412042, 989605451171, 989605463401; UDI: (01)00884838061484(21)B1X9ZR, (01)00884838061484(21)B2Y9KT, (01)00884838061484(21)B30VBJ, (01)00884838061484(21)F001VD, (01)00884838061583(21)B1XBZR, (01)00884838061644(21)B1NM93, (01)00884838061644(21)B1NM97, (01)00884838061644(21)B1PKN3, (01)00884838061644(21)B1PKNX, (01)00884838061644(21)B1QC9Q, (01)00884838061644(21)B2C3WV, (01)00884838061644(21)B36X3B, (01)00884838061644(21)B3G91R, (01)04719873000043(21)B3Q2BY, (01)04719873000043(21)F0FFRZ, (01)04719873000043(21)F0HHBM, (01)04719873000043(21)F0JKV3, 010471987300004321B24KV9, (01)00884838067882(21)B32NGP, (01)00884838067882(21)B3FP9D, (01)00884838067882(21)B27L19, (01)00884838067882(21)B2D56Y, (01)00884838061491(21)B2JT8X, (01)00884838067882(21)B1N3XG, (01)00884838067882(21)B1N3Z3, (01)00884838067882(21)B2PT8J, (01)00884838067882(21)B2THVB, (01)00884838067882(21)B2THVK, (01)00884838067882(21)B2ZN60, (01)00884838067882(21)F0DYMD, (01)00884838067882(21)F0DYMR, 010088483806788221F0G3JP, 010088483806788221F0G869, 010088483806788221F0G86F, 010088483806788221F0GCX4, (01)00884838061644(21)B25L78, (01)00884838061644(21)B25L7X, (01)00884838067882(21)B3XP02, (01)00884838061644(21)B1WDL1, (01)00884838067882(21)F083L7, (01)00884838067882(21)F0JDWK, (01)00884838061484(21)B28GVF, (01)00884838061484(21)F071WF, (01)04719873000043(21)B3L8J2, (01

UPC codes

989605430652, 989605409562, 989605427122, 989605463401, 989605430651, 989605442161, 989605418963, 989605387852, 989605418701, 989605387081, 989605412042, 989605451171, 00884838061484, 00884838061583, 00884838061644, 04719873000043, 00884838067882, 00884838061491, 00884838061613, 00884838072305

Source

Official record: FDA (Device enforcement)

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

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