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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 32781–32800 of 37665 recalls

Philips Medical Systems North America Co. Phillips: The Philips EasyDiagnost Eleva with DRF. Philips Medical...

Potential for bright artifacts to appear on the patient image from a previous exposure.

FDAJul 9, 2008AZ, CA, FL +2 more• Philips Medical Systems North America Co. Phillips

Merit Medical Systems, Inc.: 12ml Control Syringe, REF/CAT No.: CCS601 Version B, Ster...

Control Syringes may be non-sterile due to holes in the packaging.

FDAJul 9, 2008CA, FL, GA +11 more• Merit Medical Systems, Inc.

Merit Medical Systems, Inc.: 12ml Control Syringe / Smart Tip, REF/CAT No.: ST601, Ste...

Control Syringes may be non-sterile due to holes in the packaging.

FDAJul 9, 2008CA, FL, GA +11 more• Merit Medical Systems, Inc.

1...1638 163916401641 1642...1884

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Alcon Laboratories, Inc: MONARCH II IOL Delivery System, Cartridge Model B, part #...

Delivery cartridge for implanting intraocular lenses is mislabeled and may result in complicated insertion and damage to the lens.

FDAJul 7, 2008Nationwide• Alcon Laboratories, Inc

Integra Pain Management: Radiation Reduction Gloves, sterile, Latex-free, Catalog ...

Radiation reduction gloves were labeled as "Latex-free", but contain natural rubber latex.

FDAJul 7, 2008AL, CA, FL +5 more• Integra Pain Management

Spectranetics Corporation: Turbo Elite 0.9mm Turbo Elite (TE) RX, Model #410-154, ti...

The catheter pouch label was incorrectly labeled with the wrong size.

FDAJul 4, 2008Nationwide• Spectranetics Corporation

Philips Healthcare Informatics, Inc.: Philips Healthcare Informatics iSite PACS (Picture Archi...

Scout line and localizer crosshair on MPR images will display in the incorrect position under certain circumstances.

FDAJul 3, 2008Nationwide• Philips Healthcare Informatics, Inc.

Stryker Communications Corp: VERTIER Surgical Table, Catalog #0788-100-000 (Standard t...

Hydraulic lines responsible for tilting the surgical table have the potential to be severed when articulating table to its lowest position, possibly resulting in the unexpected and rapid movement of the table.

FDAJul 2, 2008Nationwide• Stryker Communications Corp

Stryker Howmedica Osteonics Corp.: Scorpio Series 7000 Tibial Impactor/Extractor, Catalog nu...

Stryker Orthopaedics became aware that there is a potential inability to release the Scorpio Series 7000 Tibial Impactor/Extractor from a tibial baseplate during use.

FDAJul 2, 2008Nationwide• Stryker Howmedica Osteonics Corp.

Integra LifeSciences Corp: Integra Dermal Regeneration Template; 8 x 10 in (20 cm x ...

Product labeled with an expiration date on May 2010, while the actual expiration date should be April 2010.

FDAJul 2, 2008AL, CA, IN +2 more• Integra LifeSciences Corp

OEC Medical Systems, Inc: GE OEC 9600 C-arm Fluoroscopy System, GE Healthcare, Surg...

Secondary collimator filters may be missing on certain x-ray units. It was discovered that the secondary collimator filter on some OEC 9600 C-arms was omitted when a collimator assembly was replaced. This would reduce the filtration and therefore the Half-Value-Layer (HVL) of the X-ray beam, and may result in non-compliance with respect to Maximum Entrance Exposure Rate (EER) unless the maximum EE

FDAJul 2, 2008Nationwide• OEC Medical Systems, Inc

Paintball Gun Adapters (RAP4) – Impact Hazard (2008)

Laceration Risk

The remote line adapter is used to connect a paintball gun to a pressurized CO2 tank. The adapter is a black cylinder and is attached to a black remote line cord. "RAP4" and the "SN" (serial number) are printed on the adapters.

CPSCJul 2, 2008Nationwide• RAP4 (Real Action Paintball Inc.), of San Jose, Calif.

Spacelabs Healthcare, Incorporated: Spacelabs Medical Temperature Probe Adaptor PN-700-0031-0...

Intermittent contact of temperature probe adaptors can cause a loss of temperature monitoring which can cause a delay in care when an alarm is missed.

FDAJul 2, 2008Nationwide• Spacelabs Healthcare, Incorporated

GE Healthcare: GE Stereotaxy Positioner, model 2405544-2, for use with ...

GE Healthcare has recently become aware of x-ray emission beyond the edge of the detector primary barrier. This issue occurs when an exam is performed in a specific angulated view associated with use of the Stereotactic Positioner of your Senographe DS Acquisition system and could impact patient safety. If the Stereotactic Positioner is removed when the examination arm is at 33 degrees and, th

FDAJul 1, 2008AL, CA, CO +16 more• GE Healthcare

Abbott Laboratories Inc.: ARCHITECT/AEROSET Activated Aspartate Aminotransferase T...

This letter is to inform you that some samples may generate A-AST results of less than (<) 5 U/L or results within the reference range when actual concentration exceeds the non-Flex linearity of 1985 U/L. In other cases the following errors may be generated. -ARCHITECT cSystems: Error Code 1053 (Unable to calculate result, rate reaction linearity failure) -AEROSET: RL% Error Code Revised P

FDAJun 30, 2008Nationwide• Abbott Laboratories Inc.

Computerized Medical Systems Inc: Monaco Radiation Treatment Planning System, Monaco Releas...

Monaco: If the user selects Monte Carlo Photon as the Secondary Algorithm (to be used for final dose calculation through segments), and selects SKIP Forward button at any time during stage 2 optimization, the system may only use the pencil beam algorithm for final computation of dose even though Monte Carlo was selected. Other than specific output to the console window, there will be no other in

FDAJun 30, 2008Nationwide• Computerized Medical Systems Inc

GE Healthcare Integrated IT Solutions: GE Healthcare Centricity Perinatal (formerly QS) System -...

Patient information mix-up: When the PFILS application, configured with a backup server has experienced a network interruption, PFILS verify could result in the Centricity Perinatal application recording non-identifiable patient information to the incorrect patient file.

FDAJun 30, 2008PR• GE Healthcare Integrated IT Solutions

Acrymed Incorporated: ON-Q Silver Dressing is a Antimicrobial wound dressing co...

The Silver Dressing, lot H0705J and H0706J may contain dressings that are not properly sealed in the foil pouch, which could affect sterility of the dressing.

FDAJun 30, 2008Nationwide• Acrymed Incorporated

Abbott Laboratories: Flexiflo Quantum Pump Set with Piercing Pin and Flush Bag...

Product was incorrectly labeled as "Top-Fill Enteral Nutrition Bag" instead of "Flexiflo Quantum Pump Set."

FDAJun 27, 2008Nationwide• Abbott Laboratories

RXV Golf Cars (E-Z-GO) – Fall Hazard (2008)

This recall involves electric and gasoline-powered Fleet RXV, Freedom RXV and RXV Shuttle 2+2 golf cars. The model names and the E-Z-GO logo are printed on the sides and front panel of all three vehicles. Serial numbers ranging from 9300001 to 9300188 and 5000000 to 5021328 are printed on a plate attached to the steering column, and the front and rear frames.

CPSCJun 27, 2008Nationwide• E-Z-GO, of Augusta, Ga. (a Textron Company)