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Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America Recalls

All product recalls associated with Philips Medical Systems Sales & Service Region No. America.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

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 36201–36220 of 37661 recalls

Philips Medical Systems Sales & Service Region No. America: EasyDiagnost Eleva Part Number 989605071921

When reviewing images in the module before sending them to PACS or printer the order can be erratic and out of sequence and may cause confusion with the interpretation of the examination.

FDAJun 8, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

Dade Behring Inc. Rte 896, Glasgow Business Community: Berichrom Heparin Reagent (OWLD11). The reagent is a co...

Customers have reported a high rate of instrument error flags and calibration issues when using affected reagent.

FDAJun 7, 2004AZ, CA, CO +20 more• Dade Behring Inc. Rte 896, Glasgow Business Community

Arrow International Inc: ARROW EPIDURAL CATHETERIZATION KIT. Product No. MC-05001.

The recall is due to a confirmed packaging error of the wrong epidural needle (longer than stated).

1...1809 181018111812 1813...1884

Page 1811 of 1884Next

FDA

Jun 7, 2004

IN, TN, TX

• Arrow International Inc

The Contact Lens Store, Inc.: Private Eyes, Diam 14.0 BC 8.6, Contents: one sterile dai...

The contact lenses were repacked in vials that were not sterile as indicated on the vial labeling.

FDAJun 7, 2004MA, TX, WA• The Contact Lens Store, Inc.

Ethicon Endo-Surgery: LIGACLIP ERCA Endoscopic Rotating Multiple Clip Applier ...

This device is subject to recall due to an increased possibility of clip scissoring which can result in less than optimal clip formation which may or may not securely ligate tubular structures.

FDAJun 7, 2004Nationwide• Ethicon Endo-Surgery

Toshiba American Med Sys Inc: Magnetic Resonance Imaging System(s) Visart and Exelar...

Fire/Burn Risk

Wrong positioning may cause patient burns.

FDAJun 7, 2004Nationwide• Toshiba American Med Sys Inc

Bio-Rad Laboratories Inc: Bio-Rad brand ''TOX/See Drug Screen Test''; Catalog numb...

The device was producing false negative results for cocaine tests.

FDAJun 4, 2004IN• Bio-Rad Laboratories Inc

Carl Zeiss Ophthalmic Systems Inc: Surgical powered laser instrument, used for photocoagulat...

Fire/Burn Risk

The coating of laser mirrors in a defined manufacturing lot of the Visulink 532/U devices may partially tear open and loosen from the base plate. The mirror may misdirect the laser beam to an unintended target in or on the eye. Retinal bleeding and burns may result.

FDAJun 3, 2004OR• Carl Zeiss Ophthalmic Systems Inc

Kuru Kuru Hair Dryers (National Electric, of Japan) – shock hazard (2004)

Laceration Risk

The recalled Kuru Kuru model hair dryers include the following model numbers: EHP798P, EHP790P, EH724V, and EH725PK. The model name and number can be found on the handle. The recalled units, which come in blue and pink, do not have an immersion protection device at the end of the plug.

CPSCJun 3, 2004Nationwide• National Electric, of Japan

Room Air Conditioning and Heating Units (Electrolux Home Products Inc., of Cleveland, Ohio) – fire hazard (2004)

Fire/Burn Risk

The recalled air conditioning/heating units are installed "thru-the-wall" and include the Frigidaire FAH12EM21 model and Carrier models 52FED31201AA.. The model numbers can be found on a serial plate on the side of the unit. The beige AC/heating units are about 14" high, 24" wide, and 20" in depth.

CPSCJun 3, 2004Nationwide• Electrolux Home Products Inc., of Cleveland, Ohio

Dream On Me Baby Walkers (Dream On Me Industries, of Brooklyn, N.Y.) – fall hazard (2004)

The recalled baby walkers have model number 408 or 423 written on a label sewn into the seats. Model 408 has a white and black tray and a black printed fabric base and seat, measuring about 25 inches by 28 inches. Model 423 has a red tray and a purple plastic base measuring about 25 inches by 28 inches. Both models have eight snap-in wheels and a label sewn into the seat that reads "DREAM ON ME IND INC. BROOKYN, NY 112321, MADE IN CHINA."

CPSCJun 2, 2004Nationwide• Dream On Me Industries, of Brooklyn, N.Y.

Smart Fit™ and Teeny Toes™ Athletic Shoes (Payless ShoeSource Inc., of Topeka, Kan.) – metal contamination (2004)

Choking Hazard

These are children's athletic shoes in prewalk and toddler sizes. The shoes are white with different color trim and come in sizes 0 to 10. The brand name "Smart Fit" or "Teeny Toes" is written on the sole and insole of the shoes. The recalled shoes have one of the following five-digit numbers, found on a label on the bottom of the shoe tongue: 31056, 31057, 31219, 32264, 32265, 33060 and 33061. No other styles or models are included in this recall.

CPSCJun 2, 2004Nationwide• Payless ShoeSource Inc., of Topeka, Kan.

Toshiba American Med Sys Inc: Pinhole Collimator (NDCL709A) for Digital Gamma Cameras G...

Pinhole collimator defective.

FDAMay 31, 2004Nationwide• Toshiba American Med Sys Inc

Abbott Health Products, Inc.: TDx/TDxFLx Opiates Reagent, Product list number: 9673-60

Abbott Diagnostics Division has found that the oxymorphone cross-reactivity information in the 'Specific Performance Characteristics' section of the TDx/TDxFLx Opiates Reagent package insert (commodity number 32-2087/R5) does not match the current product performance.

FDAMay 28, 2004Nationwide• Abbott Health Products, Inc.

CTI PET Systems Inc: PET/CT Software Versions MSV 1.0 and 1.1 used in the foll...

Misalignment of CT and PET scans from performing additional CT scans may produce an incorrect fused data set. In performing additional CT scans, the original PET and CT scans may become misaligned and produce an incorrect fused data set.

FDAMay 27, 2004Nationwide• CTI PET Systems Inc

Varian Medical Systems Inc: Linear accelerator workstation software suite

An anomaly occurs in the software suite (Millennium MLC Workstation v 6.3 and 6.4, Integrated Treat v.6.5) when used in combination with the standard series MLC controller software v 5.0 or 5.1

FDAMay 27, 2004Nationwide• Varian Medical Systems Inc

Dread Pirate coffee table game (Front Porch Classics of Seattle, Washington) – metal contamination (2004)

The "Old Century Dread Pirate™" coffee table game has many playing pieces illustrating pirates, ships, coins, and treasure. This recall covers all games with lot numbers 75, 79, and 81. The lot numbers are on the bottom of the "treasure chest."

CPSCMay 27, 2004Nationwide• Front Porch Classics of Seattle, Washington

Turbo Power electric hand-held hair dryers (Turbo Power Inc., of Flushing, New York) – shock hazard (2004)

Laceration Risk

The following hair dryers are recalled: Turbo 1500, Twin Turbo 2600, Turbo 2800 Silverado, Twin Turbo 2800, Mega Turbo 2500, Twin Turbo Ionic 3000, Parlux 3000, Mega Turbo 3000, Coldmatic 1500, Turbo Millennium 2000, Turbo 2200, and Super Turbo 1900. These hair dryers have pistol grips and have black, black and red, black and gray, or red and ivory plastic casing. They have two-prong power cords. The hair dryers are labeled in part: "Turbo Power" or "PIBBS" followed by the model number and this voltage marking: "110V/60HZ." The boxes in which the hair dryers were sold said "Made in Italy."

CPSCMay 27, 2004Nationwide• Turbo Power Inc., of Flushing, New York

Coast Mountain Spas (Coast Mountain® Spas, of Langley, British Columbia, Canada) – fire hazard (2004)

Fire/Burn Risk

The recalled Coast Mountain® spas have various model names, including Cypress, Seymour, Cowichan, Washington and Robson spas. The model name is located on the top corner of the spa. The recalled units have a capacitor made by Motors Capacitor Inc., which can be identified by a label on the motor that has the words, "Tiny Might." The spas have an acrylic liner with western red cedar siding and seat up to six adults.

CPSCMay 27, 2004Nationwide• Coast Mountain® Spas, of Langley, British Columbia, Canada

OKIFAX® 5780, 5980, 5980DL and Konica 9880 Facsimile mach... (Oki Data Americas Inc., of Mt. Laurel, N.J.) – the recalled fax machines include the... (2004)

The recalled fax machines include the OKIFAX® 5780, 5980, 5980DL models, and Konica 9880 model (manufactured by Oki Data Americas Inc.), with serial numbers beginning with 3110A, 311A, 312A, 401A and 402A. The model number is found on the top right hand side on the front of the unit and the serial numbers can be found on the back of the unit, bottom of case, centered, on the black and white bar code label.

CPSCMay 26, 2004Nationwide• Oki Data Americas Inc., of Mt. Laurel, N.J.