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Hermes Medical Solutions AB Strandbergsgatan 16 Stockholm Sweden

Hermes Medical Solutions AB Strandbergsgatan 16 Stockholm Sweden Recalls

All product recalls associated with Hermes Medical Solutions AB Strandbergsgatan 16 Stockholm Sweden.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 1681–1700 of 25000 recalls

Hybrid Recon Software (Hermes Medical) – reconstruction alignment risk (2024)

Due a potential software/configuration issue that may result is incorrect alignment during reconstructing a SPECT/CT study.

Moderate

FDAOct 31, 2024CA, CT, FL +12 more• Hermes Medical Solutions AB Strandbergsgatan 16 Stockholm Sweden

Xelstrym (Noven) – Defective Delivery System (2024)

Defective Delivery System: The product does not meet predetermined specifications for Coldflow (adhesive).

Class IIModerate

FDAOct 31, 2024Nationwide• Noven Pharmaceuticals Inc

Hannaford Seafood Salad (R. Walters Foods) – Undeclared Soy (2024)

Undeclared Allergen

Product contains undeclared hydrolyzed soy protein.

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Class II

Moderate

FDAOct 29, 2024ME, MA, NH +2 more• R. Walters Foods, Limited Liability Corporation

Dapsone Gel (Viona) – Crystallization (2024)

Crystallization

Class IIModerate

FDAOct 29, 2024Nationwide• VIONA PHARMACEUTICALS INC

Tomographic Imager (GE Medical) – acoustic noise risk (2024)

Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.

Moderate

FDAOct 28, 2024Nationwide• GE Medical Systems, LLC

Tempus LS-Manual Defibrillator (Remote Diagnostic) – incorrect labeling (2024)

Due to incorrect labels applied to devices during servicing. Labels contain the incorrect product name and CAT number.

Low

FDAOct 28, 2024Nationwide• Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom

Galaxy Bronchoscopic System (Noah Medical) – power supply failure risk (2024)

Bronchoscopic visualization system power supplies have defective semiconductor components that may fail unexpectedly, which could result in an aborted procedure since it is a non recoverable failure. Manual removal of the bronchoscope when the system is not functioning can increase the chance of injury to the tissues of the lung as the scope is withdrawn including the possibility of pneumothorax.

High

FDAOct 28, 2024CA, CT, ID +12 more• Noah Medical

Discovery MR750w 3.0T Scanner (GE Medical) – acoustic noise risk (2024)

Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.

Moderate

FDAOct 28, 2024Nationwide• GE Medical Systems, LLC

SIGNA Architect AIR MRI (GE Medical) – acoustic noise risk (2024)

Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.

Moderate

FDAOct 28, 2024Nationwide• GE Medical Systems, LLC

SIGNA Architect MRI System (GE Medical) – acoustic noise risk (2024)

Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.

Moderate

FDAOct 28, 2024Nationwide• GE Medical Systems, LLC

Galaxy System (Noah Medical) – power supply circuit risk (2024)

Bronchoscopic system uninterruptable power may have defective component, may cause power supply short circuit/trip protective circuit breakers causing sudden, unrecoverable power loss, which could occur while system is on mains or internal battery power; if during procedure, could cause interrupted/aborted procedure, may necessitate manual removal, which could lead to lung injury/pneumothorax.

High

FDAOct 25, 2024CA, CT, ID +13 more• Noah Medical

Galaxy Bronchoscope (Noah Medical) – biopsy tool compatibility issue (2024)

Not all biopsy tools meant to fit bronchoscope channel (2.1mm inner diameter/length greater or equal to 1100mm) will pass through if scope channel positioned in sharp bend (approx. greater than 100-deg.), excessive force may result in tissue injury/pneumothorax; instruments with long rigid distal sections may exhibit insertion resistance when bronchoscope bending section significantly articulated.

Moderate

FDAOct 25, 2024Nationwide• Noah Medical

BELEVINI Dried Fruit Mix (MAMTAKIM) – Undeclared Sulfites (2024)

Undeclared Allergen

Product contains undeclared sulfites. The product was sampled by the NYSAGM s Food Safety Division and tested positive at 120.7 PPM Sulfites.

Class IIModerate

FDAOct 25, 2024NJ, NY• MAMTAKIM, Inc.

Lisdexamfetamine Capsules (Lannett) – Content Uniformity (2024)

Failed Content Uniformity Specifications: Product failed to meet the action limits for stratified content uniformity.

Class IIModerate

FDAOct 25, 2024Nationwide• Lannett Company Inc.

Proteus XR/A Radiographic System (GE Healthcare) – wall stand cable risk (2024)

Steel cables in the Wall Stand for certain Proteus XR/a systems serviced by GE HealthCare have not been replaced at the intervals detailed in the Preventative Maintenance Action List.

Moderate

FDAOct 24, 2024Nationwide• GE Healthcare (China) Co., Ltd. 1F-5F BLD 1, No.1 Tongji South Road, Beijing Economic-Technological Development Area Beijing China

2025 RAM 1500 (RAM) – wheel hub encoder ring damage (2024)

Chrysler (FCA US, LLC) is recalling certain 2025 Ram 1500 vehicles. The front wheel hub encoder rings may be damaged, which can disable the electronic stability control system. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 126, "Electronic Stability Control Systems."

High

NHTSAOct 24, 2024Nationwide• RAM

Ricky Powersports ATVs (Jiangsu Tiking) – Injury Risk (2024)

Laceration Risk

The recall involves Ricky Powersports Tumble Weed youth ATVs, model TK-110ATV-1, and TGB Blade 600 SE adult ATVs. The Tumble Weed vehicles were sold in burgundy, purple camo, red spider, blue, black, blue spider, black spider, pink camo, leaf camo and army green camo colors and are intended for use by children ages 6 years and older. The model number is printed on an identification plate located at the front of the vehicle between the two front tires. The TGB Blade 600 SE ATVs were sold in black and are intended for use by adults ages 16 years and older. The model number is printed on an identification plate located next to the vehicle's front right tire. Identification plates on both models state "this ATV is subject to Ricky Powersports LLC's action plan approved by the U.S. Consumer Product Safety Commission."

High

CPSCOct 24, 2024Nationwide• Jiangsu Tiking Sports Vehicle Manufacturing Co. Ltd., of China (youth ATV)