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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.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 32341–32360 of 37665 recalls

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.

FDADec 10, 2008Nationwide• 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

St. Jude Medical Inc: Epicor LP Connecting Cable, CC-6-LP-CE, Catalog Number 12...

Firm has received multiple reports of difficulties connecting the product and/or the presence of error code messages occurring with the use of the connecting cable and the Ablation Control System unit.

1...1616 161716181619 1620...1884

Page 1618 of 1884Next

FDA

Dec 9, 2008

CA, FL, IL +8 more

• St. Jude Medical Inc

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

Ethicon Endo-Surgery Inc: Ethicon Endo-Surgery ENDOPATH Electrosurgery Probe Plus I...

Nickel exposure: The stainless steel tips on the affected product were degrading, causing a small amount of nickel to be released, which may lead to health risks in some patients, particularly those with a known or suspected nickel allergy or sensitivity. Ethicon Endo-Surgery determined the presence of free nickel in the affected product could elicit a reaction in those patients with nickel sens

FDADec 9, 2008PR• Ethicon Endo-Surgery Inc

Bio-Rad Laboratories Inc: Bio-Rad Variant II Hemoglobin Testing System with CDM v 4...

The wrong barcode number and tube position number may be assigned to samples leading to discrepant sample results.

FDADec 9, 2008Nationwide• Bio-Rad Laboratories 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.

Theragenics Corporation: Spacers of varying lengths used with the InSTANT Strandin...

Some pouches were found to have weak seals potentially compromising sterility.

FDADec 8, 2008Nationwide• Theragenics Corporation

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

Groovy Fashions Sassy Jammies Doll Clothes (Manhattan) – Lead Paint (2008)

The recalled doll clothing set features a two-piece pajama set, eye mask and slippers. The pajama top is pink satin and the pants are dark brown with multiple-colored flowers printed on them.

CPSCDec 3, 2008Nationwide• Manhattan Group, of Minneapolis, Minn.

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