Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips Recalls

All product recalls associated with Philips Medical Systems North America Co. Phillips.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

893

Class I (Serious)

124

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 15181–15200 of 17593 recalls

Philips Medical Systems North America Co. Phillips: Allura XPER FD20

Tube failure occurs involving fluoroscopy of large patients and a partial failure of the grid switch.

FDADec 10, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: EasyDiagnost Eleva x-ray systems

Tube failure occurs involving fluoroscopy of large patients and a partial failure of the grid switch.

FDADec 10, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Integris XPER FD10 F/C

Tube failure occurs involving fluoroscopy of large patients and a partial failure of the grid switch.

FDA

1...758 759760761 762...880

Page 760 of 880Next

Dec 10, 2008

Nationwide

• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Allura XPER FD20/10

Tube failure occurs involving fluoroscopy of large patients and a partial failure of the grid switch.

FDADec 10, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Computerized Medical Systems Inc: XiO Radiation Treatment Planning System, XiO Release 4.3....

XiO Software: Under certain conditions, when the port shape is altered, dose is not recalculated. The port-change flag is not being set correctly when the port shape is regenerated. The dose distribution will not match the blocking displayed and the mis-match might not be obvious. Monitor Unit calculations will also be based on an incorrect dose distribution. This problem has existed since Re

FDADec 9, 2008Nationwide• Computerized Medical Systems Inc

Smiths Medical MD, Inc.: CADD Medication Cassette Reservoir 100 ml with Clamp and ...

Smiths Medical noticed an increased trend in leakage associated with 100 ml CADD Medication Cassette Reservoirs Reorder Number 21-7002-24 Lot Numbers 213X18 and 214X18. If a leak occurs in a CADD medication Cassette Reservoir, it may allow spillage of medication, contamination of the fluid path, and/or air to enter the Reservoir. Smiths Medical has not received any report of patient injuries due

FDADec 9, 2008PA• Smiths Medical MD, Inc.

Bausch & Lomb Inc: Adapt AO, Akreos Advanced Optics Aspheric Lens. Bausch & ...

Affected lenses were inadvertently shipped to Bausch & Lomb's European Logistics Center (ELC) prior to release authorization. Initial testing indicated the product did not meet release criteria for endotoxin limits.

FDADec 8, 2008Nationwide• Bausch & Lomb Inc

American Medical Systems: AMS InteXen LP Collagen Dermal Matrix, REF 72404066. P...

The product size shown on the carton labeling does not match the size on the product inside.

FDADec 5, 2008Nationwide• American Medical Systems

C.R. Bard Access Systems, Inc: Bard Access Systems, Inc., Ponsky* PEG (Percutaneous Endo...

Snare can detach in patient. The Polypectomy Snares and the Entake Peg System (which contain these snares) are being recalled because the looped portion of the snare can become detached and drop into the stomach or other internal canal during use, necessitating retrieval of the remaining piece.

FDADec 4, 2008Nationwide• C.R. Bard Access Systems, Inc

C.R. Bard Access Systems, Inc: Bard Access Systems, Inc., Gauderer Genie* II PEG (Percut...

FDADec 4, 2008Nationwide• C.R. Bard Access Systems, Inc

C.R. Bard Access Systems, Inc: Bard Access Systems, Inc., FASTRAC "Pull" Gastric Access ...

FDADec 4, 2008Nationwide• C.R. Bard Access Systems, Inc

C.R. Bard Access Systems, Inc: Bard Access Systems, Inc., Bard* Deluxe Guidewire PEG (Pe...

FDADec 4, 2008Nationwide• C.R. Bard Access Systems, Inc

C.R. Bard Access Systems, Inc: Bard Access Systems, Inc., Fastrac* "Pull" Gastric Access...

The Polypectomy Snares and the Entake Peg System (which contain these snares) are being recalled because the looped portion of the snare can become detached and drop into the stomach or other internal canal during use, necessitating retrieval of the remaining piece.

FDADec 4, 2008Nationwide• C.R. Bard Access Systems, Inc

C.R. Bard Access Systems, Inc: Bard Access Systems, Inc., Bard* PEG (Percutaneous Endosc...

FDADec 4, 2008Nationwide• C.R. Bard Access Systems, Inc

C.R. Bard Access Systems, Inc: Bard Access Systems, Inc., Ponsky* PEG (Percutaneous Endo...

FDADec 4, 2008Nationwide• C.R. Bard Access Systems, Inc

Computerized Medical Systems Inc: Interplant Radiation Treatment Planning System, Interplan...

Interplant Software: If the trajectory needle with a non-zero retraction is adjusted in any of the planning views (Transverse, 3D) and the program is closed and reopened, the Needle Definitions page in the Dose Plan Summary (Plan View) displays the needle with a 0.00 retraction even when the needle is displayed correctly in the planning view. If the Eliminate Leading Spacers function is applied t

FDADec 1, 2008Nationwide• Computerized Medical Systems Inc

GE Medical Systems, LLC: GE Healthcare CT/e and HiSpeed X/i, families of computed ...

During internal testing, GE Healthcare has recently determined that the collimator used on our CT/e and HiSpeed X/i families of Computed Tomography systems does not comply with the specific requirements in United States Title 21 of the Code of Federal Regulations, and IEC 60601-1-3, related to leakage radiation from the diagnostic source assembly, which includes the collimator. The excess leak

FDADec 1, 2008Nationwide• GE Medical Systems, LLC

GE Medical Systems, LLC: Sytec 6000, Sytec 8000, and Lemage/ProSeed/ProSpeed famil...

FDADec 1, 2008Nationwide• GE Medical Systems, LLC

Edwards Lifesciences Research Medical, Inc.: CardioVations Ethicon, a Johnson and Johnson company, End...

Balloon rupture: Catheter balloon may rupture during cardiopulmonary bypass procedure. For further information, please telephone Edwards Lifesciences Research Medical, Inc. at 801-565-6173.

FDANov 26, 2008AL, AK, CA +32 more• Edwards Lifesciences Research Medical, Inc.

Edwards Lifesciences Research Medical, Inc.: Edwards Lifesciences CardioVations, EndoClamp aortic cath...

Balloon rupture: Catheter balloon may rupture during cardiopulmonary bypass procedure. For further information, please telephone Edwards Lifesciences Research Medical, Inc. at 801-565-6173.

FDANov 26, 2008AL, AK, CA +32 more• Edwards Lifesciences Research Medical, Inc.