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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

592

Class I (Serious)

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 2821–2840 of 10393 recalls

Atellica CH Hemoglobin A1c (Siemens) – Reagent Carryover (2022)

Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent carryover impacting quality control (QC), patient samples, and calibrator results.

FDAFeb 9, 2022Nationwide• Siemens Healthcare Diagnostics, Inc.

Atellica CH Lithium_2 (Siemens) – Reagent Carryover (2022)

Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent carryover impacting quality control (QC), patient samples, and calibrator results.

FDAFeb 9, 2022Nationwide• Siemens Healthcare Diagnostics, Inc.

DARCO Locking Bone Plate (Wright Medical) – Incorrect Date Labeling (2022)

Product was labelled with the incorrect manufacturing and distribution dates.

FDA

1...140 141142143 144...520

Page 142 of 520Next

Feb 9, 2022

• Wright Medical Technology, Inc.

Holiday House 24TB (Holiday House) – LPG System (2022)

Fire/Burn Risk

Holiday House, LLC (Holiday House) is recalling certain 2019-2021 27RQ, 24TB, and 18RB travel trailers, equipped with Winntec model 6020 two-stage propane regulators. The regulator may fail, causing an increase in propane pressure.

NHTSAFeb 8, 2022Nationwide• HOLIDAY HOUSE

Autoclavable Temperature Probes (Philips) – Cleaning Update (2022)

Update to instructions for use regarding the cleaning and disinfection process for the reusable probes.

FDAFeb 7, 2022Nationwide• Philips North America, LLC

Jaguar Power Honey (Mohammad Mayha) – hidden drug ingredient (2022)

Contains hidden drug ingredient

Class IHigh

FDAFeb 7, 2022Nationwide• Mohammad Mayha

Helmi Honey VIP (Mohammad Mayha) – hidden drug ingredient (2022)

Contains hidden drug ingredient

Class IHigh

FDAFeb 7, 2022Nationwide• Mohammad Mayha

Smart Pads Cartridge Infant/Child (Philips) – Gel Separation (2022)

There is a potential for AED pads to experience gel separation from the foam/tin backing when peeled from the plastic liner. The gel may fold onto itself resulting in reduced surface area or gel on the pad, or it may separate almost completely leaving only a small amount of gel on the pad.

FDAFeb 4, 2022Nationwide• Philips North America LLC

Smart Pads Cartridge Adult (Philips) – Gel Separation (2022)

FDAFeb 4, 2022Nationwide• Philips North America LLC

Highland Ridge TT Olympia (Highland Ridge) – Electrical Box Issue (2022)

Highland Ridge RV (Highland Ridge) is recalling certain 2022 Olympia, and Olympia Sport recreational vehicles. The metallic electrical box may not be grounded.

NHTSAFeb 3, 2022Nationwide• HIGHLAND RIDGE TT

Philips Allura (Philips) – Software Image Processing (2022)

Due to a software defect, the Philips StentBoost Live R2.0 might not process X-ray images of the current run and instead show an image processed in a previous run. The image shown could be from the same patient or from a different patient.

FDAFeb 2, 2022Nationwide• Philips North America Llc

StentBoost Live R2.0 (Philips) – Acquisition Stop Failure (2022)

Due to an incorrect configuration setting in the EPX database of StentBoost Live, acquisition does not stop automatically as it should. When the user selects the StentBoost Live protocol on the Philips Azurion system, the following on-screen message is displayed to the user in the Philips StentBoost Live application: "Press the cine pedal until the acquisition stops". However, due to the incorrect configuration of the EPX database, the acquisition does not stop after 40 images, but instead it continues as long as the pedal is pressed.

FDAFeb 2, 2022Nationwide• Philips Healthcare

Roasted Salted Cashews (Honey Heaven) – Mislabeled Nuts (2022)

Hazelnuts were packaged and mis-labeled as cashews. Hazelnuts are visible through the package.

Class IIModerate

FDAFeb 1, 2022CA, IN, OR +1 more• Honey Heaven Wholesale Inc

STANDARD Q COVID-19 Ag Home Test (SD Biosensor) – Unauthorized Import (2022)

Illegal importation of COVID-19 AG Test kits into the U.S. The COVID-19 Ag Test are not approved, cleared or authorized for distribution within the U.S.

FDAJan 31, 2022Nationwide• SD Biosensor, Inc. 1556 Beon-Gil, Yeongtong C4th & 5th Floor Digital Empire

Dimension Vista Magnesium Flex (Siemens) – Reagent Imprecision (2022)

Dimension Vista Magnesium Flex reagent cartridge lots exhibiting imprecision and intermittent Abnormal Assay flags. When this issue occurs, there is a potential for QC failures or erroneous patient results which may lead to repeat and follow-up testing.

FDAJan 28, 2022Nationwide• Siemens Healthcare Diagnostics, Inc.

CARESCAPE Central Station (GE Healthcare) – Audio Alarm Risk (2022)

If the CARESCAPE Central Station v2.0 is used with an unapproved keyboard, the audio can be muted resulting in loss of audible alarms.

FDAJan 28, 2022Nationwide• GE Healthcare, LLC

Tempus LS (Remote Diagnostic) – Unauthorized Distribution (2022)

Distribution of Defibrillators that are not approved or cleared for distribution US Market.

FDAJan 28, 2022Nationwide• Remote Diagnostic Technologies Ltd. PAVILION C2, ASHWOOD PARK ASHWOOD WAY Basingstoke United Kingdom

Meloxicam Tablets (Cardinal Healthcare) – temperature deviation (2022)

CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.

Class IIModerate

FDAJan 26, 2022Nationwide• CARDINAL HEALTHCARE

Chlorthalidone Tablets (Cardinal Healthcare) – temperature deviation (2022)

CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.

Class IIModerate

FDAJan 26, 2022Nationwide• CARDINAL HEALTHCARE

Lithium Carbonate Tablets (Cardinal) – Temperature Exposure (2022)

CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.

Class IIModerate

FDAJan 26, 2022Nationwide• CARDINAL HEALTHCARE