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Philips Healthcare Inc.

Philips Healthcare Inc. Recalls

All product recalls associated with Philips Healthcare Inc..

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Recall Summary

Total Recalls

1000

Past Year

593

Class I (Serious)

65

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 9061–9080 of 10391 recalls

Philips Healthcare Inc.: SureSigns Vital Signs Viewer (VSV):Spot Check Vital Signs...

Use of these devices at their maximum volume setting may result in the premature failure of the internal speaker

FDAOct 30, 2009Nationwide• Philips Healthcare Inc.

Siemens Healthcare Diagnostics Inc: RapidPoint 405 System Analyzers The RP405 is capable of ...

Software: Reference sensor failure may result in inaccurate pH reuslts

FDAOct 30, 2009PR• Siemens Healthcare Diagnostics Inc

Siemens Healthcare Diagnostics Inc: RapidPoint 400 Analyzers for Blood Gas, Electrolytes and ...

Software: Reference sensor failure may result in inaccurate pH reuslts

FDAOct 30, 2009PR• Siemens Healthcare Diagnostics Inc

1...452 453454455 456...520

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Philips Healthcare Inc.: SureSigns Vital Signs Monitors (VS3)-Vital Signs Viewer C...

Use of these devices at their maximum volume setting may result in the premature failure of the internal speaker

FDAOct 30, 2009Nationwide• Philips Healthcare Inc.

Philips Healthcare Inc.: SureSigns Patient Monitors (VM3, VM4. VM6. VM8): VM3 ...

Use of these devices at their maximum volume setting may result in the premature failure of the internal speaker

FDAOct 30, 2009Nationwide• Philips Healthcare Inc.

Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals: AccuSure, U-100 30 Gauge, 1/2cc Insulin Syringe, 5/16" (8...

Needles are becoming dislodged from the barrels.

FDAOct 27, 2009Nationwide• Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals: AccuSure, U-100 29 Gauge, 1cc Insulin Syringe, 1/2" Needl...

Needles are becoming dislodged from the barrels

FDAOct 27, 2009Nationwide• Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals: AccuSure, U-100 28 Gauge, 1cc Insulin Syringe, 1/2" Needl...

Needles are becoming dislodged from the barrels.

FDAOct 27, 2009Nationwide• Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals: AccuSure, U-100 31 Gauge, 1cc Insulin Syringe, 5/16" (8mm...

Needles are becoming dislodged from the barrels.

FDAOct 27, 2009Nationwide• Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals: AccuSure, U-100 31 Gauge, 1/2cc Insulin Syringe, 5/16" (8...

Needles are becoming dislodged from the barrels.

FDAOct 27, 2009Nationwide• Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals: AccuSure, U-100 29 Gauge, 1/2cc Insulin Syringe, 1/2" Nee...

Needles are becoming dislodged from the barrels.

FDAOct 27, 2009Nationwide• Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals: AccuSure, U-100 30 Gauge, 1cc Insulin Syringe, 5/16" (8mm...

Needles are becoming dislodged from the barrels.

FDAOct 27, 2009Nationwide• Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Faux Suede Roman Shades (Whole Space) – strangulation risk (2009)

This recall involves all Faux Suede room darkening Roman shades with style number 12810A. The shades were sold in Ivory, Taupe, Gold, Plum, Wine Red, Midnight Blue, Moss Green and Dark Brown and have a head rail that measures 23, 27, 31, 35, 39 43 or 48 inches. The shades have a sticker on the head rail with the letters "WS" and "style 12810A" is printed on the packaging box.

CPSCOct 27, 2009Nationwide• Whole Space Industries LTD, of Centereach, N.Y.

Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals: AccuSure, U-100 28 Gauge, 1/2cc Insulin Syringe, 1/2" Nee...

Needles are becoming dislodged from the barrels.

FDAOct 27, 2009Nationwide• Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Spacelabs Healthcare, Incorporated: The product is a 19" Spacelabs Medical Flat Panel Display...

The Spacelabs Medical Flat Panel Display, Model 94260-19 may fail prematurely and causing the screen to go blank. This inability to view data may result in delayed patient treatment.

FDAOct 23, 2009AL, AK, AR +39 more• Spacelabs Healthcare, Incorporated

Siemens Healthcare Diagnostics, Inc.: Dimension Vista CHEM 3 calibrator is an in vitro diagnos...

patient results are depressed

FDAOct 23, 2009Nationwide• Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc.: Dimension Vista V-LYTE Fluids: Standard A catalog number ...

Results can elevate after sensor replacement. Sodium urine results can be falsely elevated 15 mmol/L within 24 hours after installation of a new sensor.

FDAOct 22, 2009Nationwide• Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc.: Dimension Vista V-LYTE Fluids: Standard B/Salt Bridge cat...

Results can elevate after sensor replacement. Sodium urine results can be falsely elevated 15 mmol/L within 24 hours after installation of a new sensor.

FDAOct 22, 2009Nationwide• Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics Inc.: IMMULITE 2000 and IMMULITE 2500 IgG/IgM Sample Diluent, C...

Laceration Risk

The recall was initiated because Siemens Healthcare Diagnostics has identified there is the potential for patient results to be biased low (-0.3 Sample to Cutoff [S/CO] ratio units) due to incompatibility of the Toxoplasma IgM kits with this particular lot of IgG/IgM Sample Diluent. All available lots of the IMMULITE 2000/2500 Toxoplasma IgM kits (L2KTM/L5KTM) are incompatible with Diluent lot 150

FDAOct 21, 2009Nationwide• Siemens Healthcare Diagnostics Inc.

Siemens Healthcare Diagnostics Inc.: IMMULITE 2000 and IMMULITE 2500 IgG/IgM Sample Diluent, C...

Laceration Risk

The recall was initiated because Siemens Healthcare Diagnostics has identified there is the potential for patient results to be biased low (-0.3 Sample to Cutoff [S/CO] ratio units) due to incompatibility of the Toxoplasma IgM kits with this particular lot of IgG/IgM Sample Diluent. All available lots of the IMMULITE 2000/2500 Toxoplasma IgM kits (L2KTM/L5KTM) are incompatible with Diluent lot 150

FDAOct 21, 2009Nationwide• Siemens Healthcare Diagnostics Inc.