PlainRecalls

Philips Ultrasound, Inc.

Compiled from official public sources by the editorial team.

132 recalls on record · Latest: Apr 1, 2026

Philips Ultrasound, Inc. Recall Insight

Philips Ultrasound, Inc. appears on 132 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.130% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Apr 1, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 0 moderate, and 50 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Sep 3, 2025 to Apr 1, 2026.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Low Apr 1, 2026

Philips S5-2 Ultrasound Transducer

FDA Devices Low Apr 1, 2026

Philips S4-1 Ultrasound Transducer

FDA Devices Low Apr 1, 2026

Philips X3-1 Ultrasound Transducer

FDA Devices Low Apr 1, 2026

Philips OMNI II TEE Ultrasound Transducer

FDA Devices Low Apr 1, 2026

Philips L17-5 Ultrasound Transducer

FDA Devices Low Apr 1, 2026

Philips Mini Multi TEE Ultrasound Transducer

FDA Devices Low Apr 1, 2026

Philips OMNI III TEE Ultrasound Transducer

FDA Devices Low Apr 1, 2026

Philips 3D6-2 Ultrasound Transducer

FDA Devices Low Apr 1, 2026

Philips X7-2 Ultrasound Transducer

FDA Devices Low Apr 1, 2026

Philips C9-4 Ultrasound Transducer

FDA Devices Low Apr 1, 2026

Philips L12-5 Ultrasound Transducer

FDA Devices Low Sep 3, 2025

TRANSDUCER L12-5 Transducer Probe

FDA Devices Low Sep 3, 2025

C6-2 Transducer Probe

FDA Devices Low Sep 3, 2025

L12-5 38mm Transducer Probe

FDA Devices Low Sep 3, 2025

C8-4v Transducer Probe

FDA Devices Low Sep 3, 2025

L9-3 Transducer Probe

FDA Devices Low Sep 3, 2025

X7-2 Transducer Probe

FDA Devices Low Sep 3, 2025

S9-2 Transducer Probe

FDA Devices Low Sep 3, 2025

C8-5 Transducer Probe

FDA Devices Low Sep 3, 2025

mC7-2 Transducer Probe

FDA Devices Low Sep 3, 2025

C5-2 Lumify Transducer Probe

FDA Devices Low Sep 3, 2025

X6-1 Transducer Probe

FDA Devices Low Sep 3, 2025

C9-3v Transducer Probe

FDA Devices Low Sep 3, 2025

L12-4 Transducer Probe

FDA Devices Low Sep 3, 2025

BP10-5ec Transducer Probe

FDA Devices Low Sep 3, 2025

SCNHD LA L7-4 HDI Transducer Probe

FDA Devices Low Sep 3, 2025

L8-4 Transducer Probe

FDA Devices Low Sep 3, 2025

7.5MHZ Endo Transducer Probe

FDA Devices Low Sep 3, 2025

L10-4LAP Transducer Probe

FDA Devices Low Sep 3, 2025

C10-4ec Transducer Probe

FDA Devices Low Sep 3, 2025

X5-1 Transducer Probe

FDA Devices Low Sep 3, 2025

C8-4v Transducer Probe

FDA Devices Low Sep 3, 2025

VL13-5 Transducer Probe

FDA Devices Low Sep 3, 2025

S4-1 Lumify Transducer Probe

FDA Devices Low Sep 3, 2025

S4-2 Transducer Probe

FDA Devices Low Sep 3, 2025

OMNI II TEE Transducer Probe

FDA Devices Low Sep 3, 2025

C9-2 Transducer Probe

FDA Devices Low Sep 3, 2025

3D9-3v Transducer Probe

FDA Devices Low Sep 3, 2025

L18-5 Transducer Probe

FDA Devices Low Sep 3, 2025

D2cwc Transducer Probe

FDA Devices Low Sep 3, 2025

mL26-8 Transducer Probe

FDA Devices Low Sep 3, 2025

C6-3 Transducer Probe

FDA Devices Low Sep 3, 2025

eL18-4 Transducer Probe

FDA Devices Low Sep 3, 2025

mC12-3 Transducer Probe

FDA Devices Low Sep 3, 2025

L15-7io Transducer Probe

FDA Devices Low Sep 3, 2025

X5-1c Transducer Probe

FDA Devices Low Sep 3, 2025

L12-4 Lumify Transducer Probe

FDA Devices Low Sep 3, 2025

S7-3t Transducer Probe

FDA Devices Low Sep 3, 2025

S5-2 Transducer Probe

FDA Devices Low Sep 3, 2025

3D6-2 Transducer Probe

Nearby Manufacturers

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.