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NordicNeuroLab AS Mollendalsveien 65c Bergen Norway

NordicNeuroLab AS Mollendalsveien 65c Bergen Norway Recalls

All product recalls associated with NordicNeuroLab AS Mollendalsveien 65c Bergen Norway.

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Recall Summary

Total Recalls

1000

Past Year

426

Class I (Serious)

54

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 1061–1080 of 4598 recalls

NordicBrainEX Software (NordicNeuroLab) – Export Results Error (2022)

When exporting merged results from the BOLD, DSC, and DCE modules of nordicBrainEx, where both the underlay and overlay originated from a multiframe dataset, the resulting output may have left/right sides flipped.

FDAJun 16, 2022Nationwide• NordicNeuroLab AS Mollendalsveien 65c Bergen Norway

Draximage MAA Kit (Jubilant) – Sterility Concern (2022)

Lack of Assurance of Sterility: Out-of-specification test results obtained for Endotoxin testing.

Class IIModerate

FDAJun 16, 2022Nationwide• Jubilant Draximage Inc

Centricity PACS Software (GE Healthcare) – Notification Processing Problem (2022)

The Event Notification Manager (ENM) functionality for certain products does not process notifications for study modifications performed on post verified exams.

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FDAJun 14, 2022Nationwide• GE Healthcare, LLC

RayStation 11B (RaySearch Laboratories) – LET Display Problem (2022)

This notice concerns two issues found related to the display of Linear Energy Transfer (LET) in RayStation 11B including some service packs. First, when using a dose threshold for an evaluation dose, LET display might be misleading. Second, a displayed beam-specific LET distribution can sometimes be out of sync with the selected beam.

FDAJun 10, 2022Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

Boric Acid Vaginal Suppositories (Wedgewood) - Unsanitary Conditions (2022)

Lack of Processing Controls: Insanitary conditions observed during recent FDA Inspection

Class IIModerate

FDAJun 10, 2022Nationwide• Wedgewood Village Pharmacy, LLC

Estriol Vaginal Cream (Wedgewood) - Unsanitary Conditions (2022)

Lack of Processing Controls: Insanitary conditions observed during recent FDA Inspection

Class IIModerate

FDAJun 10, 2022Nationwide• Wedgewood Village Pharmacy, LLC

Boric Acid Capsules (Wedgewood) - Unsanitary Conditions (2022)

Lack of Processing Controls: Insanitary conditions observed during recent FDA Inspection

Class IIModerate

FDAJun 10, 2022Nationwide• Wedgewood Village Pharmacy, LLC

Bethanechol Chloride Suspension (Wedgewood) - Unsanitary Conditions (2022)

Lack of Processing Controls: Insanitary conditions observed during recent FDA Inspection

Class IIModerate

FDAJun 10, 2022Nationwide• Wedgewood Village Pharmacy, LLC

Doxycycline Suspension (Wedgewood) - Unsanitary Conditions (2022)

Lack of Processing Controls: Insanitary conditions observed during recent FDA Inspection

Class IIModerate

FDAJun 10, 2022Nationwide• Wedgewood Village Pharmacy, LLC

Estriol Vaginal Cream (Wedgewood) - Unsanitary Conditions (2022)

Lack of Processing Controls: Insanitary conditions observed during recent FDA Inspection

Class IIModerate

FDAJun 10, 2022Nationwide• Wedgewood Village Pharmacy, LLC

Belle Vie Sparkling Water (Independent Beverage) – Undeclared Caffeine (2022)

Undeclared Allergen

Firm indicated that the product contains undeclared caffeine.

Class IIModerate

FDAJun 10, 2022CT, FL, GA +14 more• Independent Beverage Company LLC

Dodge Durango (Dodge) – ABS System Malfunction (2022)

Chrysler (FCA US, LLC) is recalling certain 2018-2019 Jeep Grand Cherokee and Dodge Durango vehicles. A malfunction in the antilock-brake system (ABS) module may illuminate the brake lights, and allow the vehicle to start and shift out of Park without the brake pedal being applied.

NHTSAJun 9, 2022Nationwide• DODGE

Hisense French Door Refrigerators – Impact Injury Risk (2022)

This recall involves Hisense USA's 26.6 cubic foot capacity stainless steel French door refrigerators with ice maker with model number HRF266N6CSE and with serial numbers C2020050100001 through C2020123109000. The brand name, model, and serial number for each unit are printed on a label located on the left side of the interior of the refrigerator, above the water dispenser. With the serial number, consumers can check to determine whether their refrigerator is included in this recall by clicking http://hisenseservice.com/recall. The refrigerators are 36 inches wide and 74 inches high.

CPSCJun 9, 2022Nationwide• Hisense USA, of Suwanee, Georgia

Centricity Universal Viewer (GE Healthcare) – Inaccurate Image Measurements (2022)

Potential to display inaccurate measurements on images in Centricity Universal Viewer Zero Footprint Client (ZFP)

FDAJun 8, 2022Nationwide• GE Healthcare, LLC

CT/PET/NM Table (GE Healthcare) – Potential Table Drop (2022)

As a result of unclear guidance in the service manual, the table can drop during a specific service activity if the wrong screws are removed by the service personnel without the appropriate table supports in place resulting in injury to service personnel.

FDAJun 2, 2022Nationwide• GE Healthcare, LLC

RayStation 9B SP1 (RaySearch) – Treatment Course Propagation Problem (2022)

An issue with propagation of treatment course information from RayStation with RayTreat to RayCare has been identified. During some workflows, information may not be propagated to RayCare.

FDAJun 1, 2022Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

Aisys CS2 Anesthesia System (GE Healthcare) – Gas Cylinder Transducer Reversal (2022)

There is a potential reversal of the O2 and air cylinder pressure transducer connections.

FDAJun 1, 2022Nationwide• GE Healthcare, LLC

Avance CS2 Anesthesia System (GE Healthcare) – Base Crack Risk (2022)

The base of the anesthesia system can have a crack and could potentially fracture resulting in a tip or overbalance of the anesthesia system. This can result in potential injury if it falls on a person.

FDAMay 27, 2022AZ, CA, CO +25 more• GE Healthcare, LLC

Endo Model Modular Femur and Tibia, PorEx. orthopedic pr... (Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany) – there is a risk that blind screws of ... (2022)

There is a risk that blind screws of the modular tibial component cannot be loosened intraoperatively. This may lead to prolongation of surgery due to an intraoperative change in procedure.

FDAMay 24, 2022AL, CA, FL +12 more• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Tibial Component Modular. orthopedic prosthesis. Model N... (Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany) – there is a risk that blind screws of ... (2022)

There is a risk that blind screws of the modular tibial component cannot be loosened intraoperatively. This may lead to prolongation of surgery due to an intraoperative change in procedure.

FDAMay 24, 2022AL, CA, FL +12 more• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany