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Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc Recalls

All product recalls associated with Philips Medical Systems (Cleveland) Inc.

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Recall Summary

Total Recalls

1000

Past Year

898

Class I (Serious)

125

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 16341–16360 of 17592 recalls

Philips Medical Systems (Cleveland) Inc: Brilliance CT (computed tomography) scanners, Big Bore co...

Brilliance Big Bore- An anomaly was identified with software version 2.0 tumor localization application when printing work sheets. this causes information regarding relative locations of marked regions of interest on the patient work sheets to be incorrect and may cause mistreatment.

FDAApr 25, 2006CA, NV• Philips Medical Systems (Cleveland) Inc

Snowmobiles (Arctic Cat) – Fire and Burn Risk (2006)

Fire/Burn Risk

The recalled fuel tanks were installed on all 2004, 2005 and 2006 Firecat and Sabercat models. The recall also includes all 2003 Firecat carbureted models. The affected models were manufactured in a variety of colors and engine sizes. However, all are included in this recall.

CPSCApr 25, 2006Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.

J. Jamner Surgical Instruments, Inc.: Ruggles Leyla Ball Joint Clamp, MODEL/CATALOG #: R2383 ...

1...816 817818819 820...880

Page 818 of 880Next

The Ruggles Leyla Ball Joint Clamp may not properly tighten onto the Rigid Holding Rod. Although this condition can be observed during assembly, if the device were to be used during surgery, any attachments to the Rigid Holding Rod could move.

FDAApr 24, 2006IL, IN, MS +2 more• J. Jamner Surgical Instruments, Inc.

Excelsior Medical Corp: 0.9% Sodium Chloride Flush Syringe, 2.5 mL. Product Cod...

The syringe manufacturer mixed a pre-printed heparin labeled flush syringe with the saline syringes.

FDAApr 24, 2006Nationwide• Excelsior Medical Corp

Emergency Smoke Hoods (EVAC) – Carbon Monoxide Risk (2006)

Fire/Burn Risk

These smoke hoods are one-time use respiratory devices that assist users with breathing, while escaping a fire. They include a transparent plastic hood that covers the user's head, and a canister that filters out toxic gases. "EVAC+™" or "EVAC-U8™" is printed on the canister.

CPSCApr 20, 2006Nationwide• Brookdale International Systems Inc., of Vancouver, British Columbia, Canada

Edwards Lifesciences Research Medical, Inc.: Duraflo Treated Aortic Perfusion Cannula with plastic tip...

Due to potential embrittlement of the plastic tip which may crack or separate during use.

FDAApr 18, 2006CA, CT, FL +7 more• Edwards Lifesciences Research Medical, Inc.

Camming Anchor (CCH) – Fall Hazard (2006)

These camming anchors or "Alien Cams" are devices used as both a precautionary measure to stop a climber in the event of falls, or it is used to actually support the climber. Climbers insert the device into cracks or crevasses in rock and it grips the sides of the crack. The recalled units are marked with a small center punch dimple at the base of the round ball where the axle goes through the cable eye. They have production dates, from November 2004 (written as 1104) through December 2005 (written as 1205), which can be found on the bottom of the handle puller.

CPSCApr 18, 2006Nationwide• Colorado Custom Hardware (CCH) Inc., of Laramie, Wyo.

Edwards Lifesciences Research Medical, Inc.: Aortic Perfusion Cannula with Metal Tip, 22 Fr. x 23 cm. ...

Due to potential embrittlement of the overmolded plastic portion of the metal tip which may crack or separate during use.

FDAApr 18, 2006CA, CT, FL +7 more• Edwards Lifesciences Research Medical, Inc.

Edwards Lifesciences Research Medical, Inc.: Aortic Perfusion Cannula with plastic tip, 22 Fr. x 28 cm...

Due to potential embrittlement of the plastic tip which may crack or separate during use.

FDAApr 18, 2006CA, CT, FL +7 more• Edwards Lifesciences Research Medical, Inc.

Beckman Coulter Inc: Coulter LH500 Hematology Analyzer: Part Numbers 178832, 1...

Beckman has confirmed that erroneous results could be reported when the workstation database crashes.

FDAApr 17, 2006Nationwide• Beckman Coulter Inc

Electric Mobility Corp: Rascal 600F and 600T scooters, unspecified power wheelchair.

The four seat mast mounting screws can loosen, causing seat to wobble. The chair seat actuator and portions of the seat can malfunction and/or break. Firm is aware of problems with the seat and injuries sustained from the powered wheelchair/scooter seat malfunction. Firm has not initiated recall, claims it is a Warranty Advisory.

FDAApr 17, 2006Nationwide• Electric Mobility Corp

Bausch & Lomb: Bausch & Lomb * ReNu with MoistureLoc, Multi-purpose sof...

Reports of Fusarium Infections among contact lens wearers.

FDAApr 13, 2006Nationwide• Bausch & Lomb

Toe-Kick Saws (Crain) – Broken Handles (2006)

Laceration Risk

The saws are used for the removal of floors or cutting flooring in the toe kick area under cabinets. Only Model 795, which has a blue handle and motor housing, is included in this recall. "Model 795" and "Crain Toe-Kick Saw" are printed on a label on the blue motor housing.

CPSCApr 13, 2006Nationwide• Crain Cutter Co. Inc., of Milpitas, Calif.

Beckman Coulter Inc: Access Immunoassay system CEA, in vitro diagnostic, Part ...

Firm has confirmed that the Access CEA Assay may generate decreased values with certain frozen platelet specimens.

FDAApr 12, 2006Nationwide• Beckman Coulter Inc

Kamiya Biomedical Company: K-ASSAY CRP(2) Reagent. Kit is labeled K-ASSAY CRP (2) L...

Kits may contain 2 vials of the same reagent instead of 1 vial of buffer reagent and 1 vial of antibody reagent

FDAApr 11, 2006Nationwide• Kamiya Biomedical Company

Snowmobiles (Polaris) – Steering Hazard (2006)

The recall includes Polaris Model Year 2006 700IQ Classic, 700 IQ Touring, Select Model Year 2005 900 Fusion, 900 RMK, 900 Switchback, Select Model Year 2006 700 IQ Fusion, RMK, and Select Model Year 2006 900 Fusion, RMK Switchback Snowmobiles with Accessory Electric Start Kits. The model and serial number (VIN) identification decal is located on the right-side of the tunnel underneath the seat. The model and serial number (VIN) identification decal is located on the right-side of the tunnel underneath the seat. The table below lists all models possibly affected by the recall. Model(s) Affected Model Numbers 2005 900 Fusion (With Accessory Electric Start Kit) S05MP8DS (A)(B)(C) 2005 900 Switchback (With Accessory Electric Start Kit) S05PS8DS 2005 900 RMK (With Accessory Electric Start Kit) S05PL8DS (A)(B)(C)(D) S05PL8DEB S05PM8DS (A)(B) S05PN8DS S05PN8DE 2006 700 Classic (Electric Start Standard) S06PD7HS 2006 700 Touring (Electric Start Standard) S06PT7HS S06PT7HE 2006 700 Fusion (With Snow Check Select Option or Accessory Electric Start Kit) S06MP7HS (A)(B) S06ME7HS 2006 700 RMK (With Snow Check Select Option or Accessory Electric Start Kit) S06PK7HS (A)(B) S06PL7HS (A)(B) S06PM7HS (A) 2006 900 Fusion (With Snow Check Select Option or Accessory Electric Start Kit) S06MP8DS (A)(B) S06ME8DS 2006 900 Switchback (With Snow Check Select Option or Accessory Electric Start Kit) S06PS8DS (A) 2006 900 RMK (With Snow Check Select Option or Accessory Electric Start Kit) S06PL8DS (A)(B) S06PM8DS (A) S06PN8DS (A) S06PR8DS Note: Not all Model Year 2005 and 2006 snowmobiles are affected.

CPSCApr 11, 2006Nationwide• Polaris Industries Inc., of Medina, Minn.

Northwest Medical Physics Equipment Inc: ISOLOC 6.5 Software Part Number NT-NW-425-520. Software ...

This correction was for several software bugs which caused image format problems; incorrect ruler display; software crashes; failure to update pixel spacing; display of unattainable treatment table positions; failure to update gantry angles; wrong shifts for two of three axes of treatment table movement.

FDAApr 7, 2006IN• Northwest Medical Physics Equipment Inc

Bard Access Systems, Inc: 20F Tri-Funnel Replacement Gastrostomy Tube

Packaging for some gastrostomy tubes was labeled with incorrect balloon inflation data. An underinflated balloon may cause misplacement, slippage or premature removal of the tube. If an underinflated balloon allows the tube to be placed, or slip into, the stomal tract and not the stomach, there is a risk of infusion of fluids into the peritoneum. This carries the risk of infection.

FDAApr 6, 2006Nationwide• Bard Access Systems, Inc

Bard Access Systems, Inc: 22F Tri-Funnel Replacement Gastrostomy Tube

FDAApr 6, 2006Nationwide• Bard Access Systems, Inc

InMotion Trampolines – Injury Risk (2006)

The round, black mini-trampoline measures 36 inches across and has six 7½-inch long metal legs. The mini-trampoline is used for in-place jogging and other cardiovascular exercises. Most mini-trampolines that have model numbers containing 35-1625 are included in the recall. Model 35-1625C and 35-1625CW units are not included in the recall. The model number, along with the customer service and serial numbers, are stamped on a black and white label on one of the legs, containing the name "Stamina."

CPSCApr 6, 2006Nationwide• Stamina Products Inc., of Springfield, Mo.