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Philips North America Llc recall records

256 reported ongoing

261 records in this archive. Latest source date Aug 7, 2026.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

Records and reported status

Nov 20, 2024FDA device enforcement

Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216

The following four issues are included: 1. Certain Channel Settings may result in an Access Point preventing a connected client device from roaming to another Access Point potentially causing the client device to appear to drop out from the network. 2. if t...

Class IIReported ongoing

Distribution: Nationwide distribution

Official source

Nov 16, 2024FDA device enforcement

Spectral CT and Spectral CT Plus. Model Numbers: 728333, 728340, 728344.

Potential for a plan box not updated issue during Interventional procedure with Spectral CT that may lead to a collision with the operator or with the needle placed inside the patient, and an incorrect patient ID software issue that may lead to misdiagnosis.

Class IIReported ongoing

Distribution: Worldwide - US Nationwide distribution in the states of AR, AZ, CA, FL, GA, HI, IN, KY, MA, MD, MN, NY, OH, OR, PA, TX, VT, WA, WV and the countries of Australia, Austria, Belgi...

Official source

Nov 4, 2024FDA device enforcement

Achieva TX Interventional Coil 3.0T

Potential safety issue where a patient may be harmed while preparing for or during a scan.

Class IIReported ongoing

Distribution: US Nationwide distribution.

Official source

Nov 4, 2024FDA device enforcement

dS Breast 16ch 1.5T

Potential safety issue where a patient may be harmed while preparing for or during a scan.

Class IIReported ongoing

Distribution: US Nationwide distribution.

Official source

Nov 4, 2024FDA device enforcement

dS Breast 16ch 3.0T

Potential safety issue where a patient may be harmed while preparing for or during a scan.

Class IIReported ongoing

Distribution: US Nationwide distribution.

Official source

Nov 4, 2024FDA device enforcement

dS Breast 7ch 1.5T

Potential safety issue where a patient may be harmed while preparing for or during a scan.

Class IIReported ongoing

Distribution: US Nationwide distribution.

Official source

Nov 4, 2024FDA device enforcement

dS Breast 7ch 3.0T

Potential safety issue where a patient may be harmed while preparing for or during a scan.

Class IIReported ongoing

Distribution: US Nationwide distribution.

Official source

Nov 4, 2024FDA device enforcement

Mammotrak Diagnostic Coil 1.5T

Potential safety issue where a patient may be harmed while preparing for or during a scan.

Class IIReported ongoing

Distribution: US Nationwide distribution.

Official source

Nov 4, 2024FDA device enforcement

Mammotrak Interventional Coil 1.5T

Potential safety issue where a patient may be harmed while preparing for or during a scan.

Class IIReported ongoing

Distribution: US Nationwide distribution.

Official source

Nov 4, 2024FDA device enforcement

Mammotrak Diagnostic Coil 3.0T

Potential safety issue where a patient may be harmed while preparing for or during a scan.

Class IIReported ongoing

Distribution: US Nationwide distribution.

Official source

Nov 4, 2024FDA device enforcement

Mammotrak Interventional Coil 3.0T

Potential safety issue where a patient may be harmed while preparing for or during a scan.

Class IIReported ongoing

Distribution: US Nationwide distribution.

Official source

Nov 4, 2024FDA device enforcement

SENSE Breast Coil

Potential safety issue where a patient may be harmed while preparing for or during a scan.

Class IIReported ongoing

Distribution: US Nationwide distribution.

Official source

Nov 4, 2024FDA device enforcement

SENSE Breast Coil 3.0T 7ch

Potential safety issue where a patient may be harmed while preparing for or during a scan.

Class IIReported ongoing

Distribution: US Nationwide distribution.

Official source

Nov 4, 2024FDA device enforcement

ST SENSE Breast Coil

Potential safety issue where a patient may be harmed while preparing for or during a scan.

Class IIReported ongoing

Distribution: US Nationwide distribution.

Official source

Nov 4, 2024FDA device enforcement

ST SENSE Breast Dx Coil

Potential safety issue where a patient may be harmed while preparing for or during a scan.

Class IIReported ongoing

Distribution: US Nationwide distribution.

Official source

Sep 3, 2024FDA device enforcement

Evolution Upgrade 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extr...

Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and protrude beyond the surface could cause the screws to interfere with other moving parts, potentially blocking the horizontal tabletop. May lead to delay in diagnosis and/or may incl...

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Belgium, Brazil, Canada, Chile, China, Colombia, Croatia, Czech Republic, Denmark, Ecuador, Egy...

Official source

Sep 3, 2024FDA device enforcement

Ingenia 1.5T -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremities, in...

Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and protrude beyond the surface could cause the screws to interfere with other moving parts, potentially blocking the horizontal tabletop. May lead to delay in diagnosis and/or may incl...

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Belgium, Brazil, Canada, Chile, China, Colombia, Croatia, Czech Republic, Denmark, Ecuador, Egy...

Official source

Sep 3, 2024FDA device enforcement

Ingenia 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremities, i...

Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and protrude beyond the surface could cause the screws to interfere with other moving parts, potentially blocking the horizontal tabletop. May lead to delay in diagnosis and/or may incl...

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Belgium, Brazil, Canada, Chile, China, Colombia, Croatia, Czech Republic, Denmark, Ecuador, Egy...

Official source

Sep 3, 2024FDA device enforcement

Ingenia 3.0T CX - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremities...

Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and protrude beyond the surface could cause the screws to interfere with other moving parts, potentially blocking the horizontal tabletop. May lead to delay in diagnosis and/or may incl...

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Belgium, Brazil, Canada, Chile, China, Colombia, Croatia, Czech Republic, Denmark, Ecuador, Egy...

Official source

Sep 3, 2024FDA device enforcement

Ingenia Ambition S - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremit...

Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and protrude beyond the surface could cause the screws to interfere with other moving parts, potentially blocking the horizontal tabletop. May lead to delay in diagnosis and/or may incl...

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Belgium, Brazil, Canada, Chile, China, Colombia, Croatia, Czech Republic, Denmark, Ecuador, Egy...

Official source

Reasons in these listed records

The following four issues are included: 1. Certain Channel Settings may result in an Access Point preventing a connected client device from roaming to another Access Point potentially causing the client device to appear to drop out from the network. 2. if the Access Point expe...
Potential for a plan box not updated issue during Interventional procedure with Spectral CT that may lead to a collision with the operator or with the needle placed inside the patient, and an incorrect patient ID software issue that may lead to misdiagnosis.
Potential safety issue where a patient may be harmed while preparing for or during a scan.
Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and protrude beyond the surface could cause the screws to interfere with other moving parts, potentially blocking the horizontal tabletop. May lead to delay in diagnosis and/or may include anxiety of a pat...

These examples come from this result page and are not a ranking of every recall reason.

Checking Philips North America Llc

Is there a recall on philips north america llc right now?

This archive contains 261 records, including 256 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. Use the label-check guide if you need help locating an identifier.

Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. Check source coverage and the agency's current notices.

Where can I find older records?

Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

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