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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 5561–5580 of 37665 recalls

ADVIA Chemistry Protein Test (Siemens) – reagent carryover (2023)

There is a potential for ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein reagent carryover impacting Enzymatic Creatinine_2 (ECRE_2). Falsely depressed ECRE_2 results may be observed when the assay is processed after the UCFP test on ADVIA Chemistry systems.

Moderate

FDAJul 25, 2023Nationwide• Siemens Healthcare Diagnostics, Inc.

Membrane Changer (SenTec) – manufacturing material risk (2023)

During rework of components during the manufacturing process, an additional piece of material may have been left in the device, which may result in an impact on measurement performance.

Low

FDAJul 25, 2023Nationwide• SenTec AG Ringstrasse 39 Therwil Switzerland

Instacure #1 (The Sausage Maker) – metal contamination (2023)

Contains Sodium Nitrite recalled for potential metal contamination

Class III

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Low

FDAJul 25, 2023Nationwide• The Sausage Maker, Inc.

O-arm O2 Imaging System (Medtronic) – ground cable problem (2023)

Ground cable installed incorrectly.

Moderate

FDAJul 25, 2023Nationwide• Medtronic Navigation, Inc.-Littleton

Trigen Trochanteric Nail (Smith & Nephew) – incorrect implant (2023)

A complaint was received indicating that a package contained a TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 40CM 130 DEGREE LEFT implant instead of a TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 36CM 130 DEGREE LEFT as described on the product label.

Moderate

FDAJul 24, 2023CA, DE, PA• Smith & Nephew, Inc.

Dark Chocolate Almond Cookies (Trader Joe's) – foreign object (2023)

Foreign object; rocks.

Class IIModerate

FDAJul 24, 2023AZ, CA, CT +5 more• Fantasy Cookie Corporation

Almond Windmill Cookies (Trader Joe's) – foreign object (2023)

Foreign object; rocks.

Class IIModerate

FDAJul 24, 2023AZ, CA, CT +5 more• Fantasy Cookie Corporation

Keystone Bosworth Copaliner Varnish (Keystone) – Packaging Error (2023)

A bottle of Copaliner Solvent was inadvertently packaged into a box labeled as Copaliner Varnish (0921526) and sold as Copaliner Varnish (0921526).

Moderate

FDAJul 21, 2023Nationwide• Keystone Industries

Forest River Impression (Forest River) – Griddle Stowage (2023)

Fire/Burn Risk

Forest River, Inc. (Forest River) is recalling certain 2023 Impression fifth wheels vehicles. The exterior griddle may be stowed while still connected to LP gas line.

High

NHTSAJul 21, 2023Nationwide• FOREST RIVER

Jersey Girl Cheese (Cooperstown Cheese Company) – Listeria Risk (2023)

Listeria

Cheese may be contaminated with Listeria monocytogenes.

Class IIModerate

FDAJul 21, 2023NY• Cooperstown Cheese Company, LLC

Cromolyn Sodium Solution (Ritedose) – Supplier Approval Issue (2023)

CGMP deviation: product released prior to supplier approval.

Class IIModerate

FDAJul 21, 2023Nationwide• The Ritedose Corporation

Green Curry Paste (Every Plate) – temperature abuse (2023)

Product spoiled due to temperature abuse.

Class IIModerate

FDAJul 21, 2023AR, IL, NJ +5 more• EVERY PLATE

Neurosurgical Trocar (Aesculap) – Manufacturing Length Issue (2023)

Trocar manufactured with the shaft too long and does not meet manufacturing specifications. As a result, when used with the 30 neuroendoscope, a portion of the visual field is obscured.

Moderate

FDAJul 20, 2023Nationwide• Aesculap Implant Systems LLC

Visera Hysterovideoscope (Olympus) – Labeling Update (2023)

IFU labeling is being updated to revise EtO gas mixture and elimination of reusable cleaning brushes.

Low

FDAJul 20, 2023Nationwide• Olympus Corporation of the Americas

Zenition 70 (Philips) – Radiation Exposure Risk (2023)

Philips has become aware of the potential for unintended radiation exposure with Zenition 70 systems with Vascular Extension option and a Wireless Foot Switch.

Moderate

FDAJul 20, 2023Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

Azurion (Philips) – Unintended Radiation Emission (2023)

A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation

Moderate

FDAJul 19, 2023Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

Allura Xper Series (Philips) – Unintended Radiation Emission (2023)

A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation

Moderate

FDAJul 19, 2023Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

Freedom Boom Models (IHB) – Suspension Arm Weakness (2023)

Weakened connection point on the adjustable suspension arm, potentially causing damage or a break.

Moderate

FDAJul 19, 2023AL, AZ, AR +33 more• IHB OPERATIONS B.V. Floresstraat 52 Zwolle Netherlands

Sportsmobile Dodge ProMaster (Sportsmobile) – Equipment Issue (2023)

Fire/Burn Risk

Sportsmobile Texas, Inc. (Sportsmobile) is recalling certain 2021 Dodge Sportsmobile Pro Master and 2021-2022 Ford Sportsmobile Transit vans equipped with Cummins Onan QG 2800i or Onan QG 2800i EVAP generator sets. The fuel hose between the inline fuel filter and the Injection Pump Module (IPM) may not be properly secured, which can cause a gas leak.

High

NHTSAJul 19, 2023Nationwide• SPORTSMOBILE

Sodium Nitrite (Chemtrade Solutions) – Metal Fragment Risk (2023)

Product may contain metal fragments (ferrous metal, 1 mm or less in size)

Class IIModerate

FDAJul 19, 2023IL, IA, MI +2 more• Chemtrade Solutions, LLC