Manufacturer

Philips Ultrasound, Inc

101 recalls in our database name Philips Ultrasound, Inc as the manufacturing or recalling firm.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–25 of 101

ModerateFDA (Devices)·Z-1627-2026·2026-04-01
Philips X3-1 Ultrasound Transducers Recalled for Useful Life Labeling Clarification
Philips Ultrasound, Inc. is recalling 17 Philips X3-1 Ultrasound Transducers nationwide to provide clarification and labeling defining the equipment's useful life. This FDA Class III recall ensures healthcare facilities have complete information about equipment specifications.
Product
Philips X3-1 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1624-2026·2026-04-01
Philips OMNI III TEE Ultrasound Transducer Labeling Clarification Recall
Philips Ultrasound is recalling 75 OMNI III TEE ultrasound transducers distributed nationwide. The recall provides clarification and updated labeling to define the devices' useful life.
Product
Philips OMNI III TEE Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1626-2026·2026-04-01
Philips S5-2 Ultrasound Transducer: Labeling Clarification on Useful Life
Philips Ultrasound is updating labeling on the S5-2 Ultrasound Transducer to clarify the useful life of the device. This is a labeling-only recall with nationwide US distribution.
Product
Philips S5-2 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1620-2026·2026-04-01
FDA clarifies useful life labeling for Philips L12-5 ultrasound transducers
Philips Ultrasound is clarifying labeling on certain L12-5 ultrasound transducers to properly define the devices' useful life in clinical use.
Product
Philips L12-5 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1622-2026·2026-04-01
Philips Mini Multi TEE Transducers Recalled for Labeling Clarification
Philips Ultrasound is recalling 11 Mini Multi TEE transducers distributed nationwide to provide clarification and labeling defining the useful life of the devices.
Product
Philips Mini Multi TEE Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1625-2026·2026-04-01
Philips S4-1 Ultrasound Transducers: Useful Life Labeling Clarification
Philips recalls 41 S4-1 ultrasound transducers sold nationwide to clarify labeling regarding useful life. No injuries or adverse events reported.
Product
Philips S4-1 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1618-2026·2026-04-01
Philips 3D6-2 Ultrasound Transducers Recalled for Labeling Clarification
Philips Ultrasound recalls 17 units of the Philips 3D6-2 Ultrasound Transducer to provide clarification and labeling that defines the device's useful life.
Product
Philips 3D6-2 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1621-2026·2026-04-01
Philips L17-5 Ultrasound Transducer Labeling Clarification Issued
Philips Ultrasound, Inc. is providing labeling clarification for the L17-5 Ultrasound Transducer to define the product's useful life.
Product
Philips L17-5 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1623-2026·2026-04-01
Philips OMNI II TEE Ultrasound Transducer Labeling Clarification for Useful Life
Philips Ultrasound is issuing a labeling clarification for two OMNI II TEE ultrasound transducers to define their useful life in clinical use.
Product
Philips OMNI II TEE Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1619-2026·2026-04-01
Philips C9-4 Ultrasound Transducer labeling clarification for device useful life
Philips Ultrasound, Inc. has recalled the C9-4 Ultrasound Transducer to provide labeling clarification regarding the device's useful life. No adverse events have been reported.
Product
Philips C9-4 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1628-2026·2026-04-01
Philips X7-2 Ultrasound Transducers recalled for useful life labeling clarification
Philips is recalling five ultrasound transducers to provide clarification and labeling regarding their useful life in clinical field use. Affected units were distributed nationwide.
Product
Philips X7-2 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2349-2025·2025-09-03
Philips BP10-5ec Ultrasound Transducer Probe Recalled for Labeling Clarification
Philips Ultrasound is recalling 171,322 BP10-5ec Transducer Probes nationwide to provide clarification on labeling that defines product useful life.
Product
BP10-5ec Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2356-2025·2025-09-03
Philips C6-3 Transducer Probe Labeling Clarification on Useful Life
Philips is providing labeling clarification to define the useful life of C6-3 Transducer Probes in the field. 171,322 units are affected nationwide.
Product
C6-3 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2387-2025·2025-09-03
Philips OMNI II TEE Transducer Probe Labeling Recall for Useful Life Clarification
Philips Ultrasound is recalling 171,322 OMNI II TEE transducer probes nationwide to provide labeling clarification on product useful life.
Product
OMNI II TEE Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2348-2025·2025-09-03
Philips 7.5MHz Endo Transducer Probe Recall for Labeling Clarification
Philips Ultrasound is clarifying labeling on 171,322 units of 7.5MHz Endo Transducer Probes to properly define device useful life. Devices were distributed nationwide.
Product
7.5MHZ Endo Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2392-2025·2025-09-03
Philips S4-1 Lumify Transducer Probe: Labeling Clarification on Useful Life
Philips is recalling the S4-1 Lumify Transducer Probe to provide clarification and labeling that defines the useful life of ultrasound transducers. The recall affects 171,322 units distributed nationwide.
Product
S4-1 Lumify Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2375-2025·2025-09-03
Philips L12-5 Transducer Probe Recalled to Clarify Useful Life Labeling
Philips Ultrasound is recalling 171,322 L12-5 Transducer Probes to clarify labeling that defines useful life. The Class III recall affects devices distributed nationwide in the US.
Product
L12-5 38mm Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2408-2025·2025-09-03
Philips X5-1 Transducer Probe Recalled for Useful Life Labeling Clarification
Philips is recalling X5-1 Transducer Probes to clarify labeling regarding the product's useful life. The manufacturer is providing updated labeling to clearly define when the device should no longer be used.
Product
X5-1 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2402-2025·2025-09-03
Philips Ultrasound L12-5 Transducer Probe Recall for Labeling Clarification
Philips is recalling 171,322 L12-5 ultrasound transducer probes distributed nationwide to provide clarification and proper labeling defining the device's useful life.
Product
TRANSDUCER L12-5 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2371-2025·2025-09-03
Philips L11-3 Ultrasound Transducer Probe Labelling Clarification
Philips is recalling 171,322 L11-3 ultrasound transducer probes to provide clarification and labelling defining the devices' useful life. Units were distributed nationwide.
Product
L11-3 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2393-2025·2025-09-03
Philips S4-2 Transducer Probe Labeling Clarification on Useful Life
Philips is clarifying labeling on S4-2 Transducer Probes to define product useful life. About 171,322 units distributed nationwide are affected.
Product
S4-2 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2384-2025·2025-09-03
FDA Recalls Philips mC7-2 Ultrasound Transducer Probe Labeling Clarification
Philips is recalling 171,322 mC7-2 Transducer Probes distributed nationwide to clarify labeling defining the useful life of ultrasound transducers. No injuries or illnesses have been reported.
Product
mC7-2 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2355-2025·2025-09-03
Philips C6-2 Ultrasound Transducer Probes Labeling Clarification on Useful Life
Philips Ultrasound issued a nationwide recall of 171,322 C6-2 Transducer Probes to provide clarification and labeling defining the useful life of these ultrasound transducers.
Product
C6-2 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2386-2025·2025-09-03
Philips Ultrasound mL26-8 Transducer Probe Labeling Clarification Recall
Philips Ultrasound is recalling 171,322 mL26-8 Transducer Probe units nationwide to provide clarification and labeling defining the useful life of these ultrasound transducers in clinical use.
Product
mL26-8 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2368-2025·2025-09-03
Philips D5cwc Ultrasound Transducers Recalled for Labeling Clarification
Philips Ultrasound is recalling 171,322 units of the D5cwc Transducer Probe nationwide to provide labeling clarification and define the product's useful life.
Product
D5cwc Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide