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Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc. Recalls

All product recalls associated with Siemens Healthcare Diagnostics, Inc..

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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 31761–31780 of 37665 recalls

Dimension Vista BUN Reagent (Siemens) - Incorrect Results (2009)

Incorrect result: patient sample BUN results reported may be higher or lower than actual level.

FDAJun 16, 2009Nationwide• Siemens Healthcare Diagnostics, Inc.

PainPump2 5.0 Catheter (Stryker) - Potential Catheter Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

PainPump ExFen Catheter (Stryker) - Potential Catheter Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

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FDA

Jun 16, 2009

Nationwide

• Stryker Instruments Div. of Stryker Corporation

PainPump 5-Day Infusion Kit (Stryker) - Potential Catheter Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

PainPump 270mL Kit (Stryker) - Potential Catheter Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

ExFen Catheter (Stryker) - Potential Catheter Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

PainPump Base Kit (Stryker) - Potential Catheter Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

PainPump 2-Day Kit (Stryker) - Potential Catheter Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

PainPump 270mL Base Kit (Stryker) - Potential Catheter Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

PainPump ExFen 2.5in Catheter (Stryker) - Potential Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

PainPump Catheter Set (Stryker) - Potential Catheter Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

PainPump2 2.5 Catheter (Stryker) - Potential Catheter Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

PainPump2 400mL Kit (Stryker) - Potential Catheter Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

PainPump2 Two-Site Kit (Stryker) - Potential Catheter Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

PainPump2 ExFen 5 (Stryker) - Potential Catheter Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

PainPump Standard Catheter (Stryker) - Potential Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

PainPump2 ExFen 2.5 (Stryker) - Potential Catheter Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

PainPump2 250mL Two-Site Kit (Stryker) - Potential Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

ExFen 2.5in Catheter (Stryker) - Potential Catheter Failure (2009)

The catheter may break when removed from the body, or the catheter may have kinks or be occluded such that the patient will not receive the intended quantity of medication.

FDAJun 16, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

Coffee Grinders (Starbucks) – laceration hazard (2009)

Laceration Risk

This recall includes the Starbucks Barista® Blade Grinders and Seattle's Best Coffee® Blade Grinders with the following colors and SKU numbers: Brand Color SKU # Starbucks Barista® Blade Grinder Stainless Steel 171884 Starbucks Barista® Blade Grinder Green 195234 Starbucks Barista® Blade Grinder Pink 195235 Starbucks Barista® Blade Grinder Orange 220623 Starbucks Barista® Blade Grinder Teal 220624 Starbucks Barista® Blade Grinder Cranberry 242275 Starbucks Barista® Blade Grinder Olive 344476 Starbucks Barista® Blade Grinder Black 454482 Seattle's Best Coffee® Blade Grinder Brown Metallic 474881

CPSCJun 16, 2009Nationwide• Tsann Kuen (Zhangzhou) Enterprise Co. Ltd. ("TKL"), of China