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RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden Recalls

All product recalls associated with RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden.

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Recall Summary

Total Recalls

1000

Past Year

579

Class I (Serious)

Most Recent

Dec 2025

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 3081–3100 of 10937 recalls

RayStation (RaySearch) - Incorrect Beam Positioning (2021)

Initial delivery positions will be set incorrectly when having setup beam(s) at the localization point.

Moderate

FDAJun 8, 2021TN• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

Recirculator 8.0s Kit (Eight Medical) - Aluminum Ion Release Risk (2021)

The patient may be exposed to potential aluminum ion release during warming therapy under certain use conditions.

Moderate

FDAJun 4, 2021Nationwide• Eight Medical International BV Laan Van Hildernisse-Noord 2a Bergen Op Zoom Netherlands

ScanIP Software (Simpleware) - Incorrect Anatomical Orientation (2021)

A issue (bug) has been identified with the interface and image software which could result in anatomical orientation tags/labels being displayed incorrectly. This could result in operator misunderstanding and errors during resampling or re-alignment of image data

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Low

FDAJun 4, 2021Nationwide• Simpleware Product Group, SYNOPSYS NORTHERN EUROPE Bradninch Hall Castle Street Exeter United Kingdom

ScanIP Software (Simpleware) - Incorrect Anatomical Orientation (2021)

Low

FDAJun 4, 2021Nationwide• Simpleware Product Group, SYNOPSYS NORTHERN EUROPE Bradninch Hall Castle Street Exeter United Kingdom

Bulkamid Urethral System (Axonics) - Sterility Assurance Concern (2021)

Lack of Sterility Assurance; needle in procedure pack labeled as sterile may not have been adequately sterilized

High

FDAJun 3, 2021Nationwide• Axonics Modulation Technologies, Inc.

StimLoc Burr Hole Cover (Medtronic) - Nylon Flash Excess (2021)

Excess nylon flash on the clip.

Moderate

FDAJun 2, 2021AL, AZ, AR +44 more• Medtronic Neuromodulation

Moderna Vaccine Kit (McKesson) - Unsuitable Syringe Risk (2021)

Two unsuitable 3mL syringes with conventional needles for vaccine administration included in some Moderna 140 Ancillary Convenience Kits.

Moderate

FDAJun 2, 2021Nationwide• Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233

Reveal LINQ (Medtronic) - Electrical Reset Malfunction (2021)

Reveal LINQ with TruRhythm ICMs, that undergo a partial electrical reset appear to be programmed "ON", but are no longer able to detect and report Brady and Pause events to clinicians.

High

FDAJun 1, 2021Nationwide• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Chemical Products (Williams Advanced Materials) - Safety Compliance (2021)

Fire/Burn Risk

This recall involves Williams Advanced Materials & Chemicals sodium hydroxide, heptane, and naphtha. The sodium hydroxide, also called lye or caustic soda, was sold in either a jar with a continuous thread cap or resealable silver bag available in one-pound, two-pound and five-pound sizes. The naphtha was sold in a metal can in one-half gallon and gallon sizes. The heptane was sold in a metal can in quart, one-half gallon and gallon sizes. The WAM&C logo and the product name are printed on a white label at the front of the product.

High

CPSCMay 27, 2021Nationwide• Williams Advanced Materials & Chemicals Inc., of Clairton, Pa.

Cytocell E2A Probe (Cytocell) – Signal Variation Risk (2021)

May show unexpected locus specific signals in addition to those at 19p13.3. Users may observe faint additional locus specific signals at 9q34

Low

FDAMay 27, 2021Nationwide• Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom

3AA Battery Cradle (Mindray) – Power On Malfunction (2021)

Telepack may not power on when using the 3AA battery cradle.

Low

FDAMay 27, 2021Nationwide• Mindray DS USA, Inc. dba Mindray North America

Proteus Therapy System (Ion Beam) – Beam Gating Issue (2021)

if the user forgets to select the trigger input manually while beam gating is prescribed for the patient, the proton irradiation will be delivered without gating. If the beam is not gated as prescribed, the treatment field may be delivered with an error in position

High

FDAMay 26, 2021FL, PA, TN +2 more• Ion Beam Applications S.A. Chemin Du Cyclotron 3 Louvain-la-neuve Belgium

Azurion Systems (Philips) – Study Addition Error (2021)

In the Azurion system, the user can add a new study to a patient by selecting the option Add Study . The Add Study dialogue box is then displayed where the Patient Type is selected to perform the study. Due to a software defect, when the study is initiated by pressing Start Procedure , the Patient Type changes inadvertently to a Patient Type different than the one selected as shown in the Table below. Patient type is one of the factors involved in the dose control process. The incorrect patient type changes the technique factors to be used by the system without notification to the user.

Moderate

FDAMay 26, 2021Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Levetiracetam Tablets (McKesson) - Barcode Error (2021)

Labeling; Wrong Barcode; error in the machine-readable barcode which could result in some units being read as Naproxen Tablets 500 mg. Product is labeled correctly as Levetiracetam

Class IIILow

FDAMay 26, 2021Nationwide• McKesson Corporation dba McKesson Drug Company

TigerNut Flour (Organic Gemini) - Salmonella Contamination (2021)

Salmonella

Product may be contaminated with Salmonella.

Class IHigh

FDAMay 26, 2021ID, KS, OR +1 more• HMO Beverage Corp. dba Organic Gemini LLC

Tempus Pro Monitor (Remote Diagnostic) – Console Transition Error (2021)

The Tempus Pro (Trizeps 7 only) when used in combination with a specified laryngoscope device can cause two error types when subsequently unplugged.

Moderate

FDAMay 25, 2021Nationwide• Remote Diagnostic Technologies Ltd. PAVILION C2, ASHWOOD PARK ASHWOOD WAY Basingstoke United Kingdom

Canon Vantage Titan 3T (Canon) – Flame Retardancy Issue (2021)

Fire/Burn Risk

The MRI system contains a component that does not meet the appropriate flame retardancy-rating which could result in smoke or fire.

High

FDAMay 21, 2021Nationwide• Canon Medical System, USA, INC.

Rugged Mountain K2 (Rugged Mountain) – Stove Valve Risk (2021)

Fire/Burn Risk

Tiny Idahomes LLC (Tiny Idahomes) is recalling certain 2019 RMCRV K2 trailers equipped with Dometic 3-burner cooking stoves. The saddle valve securing bolt may be overtightened, possibly damaging the o-ring seal and causing a continuous gas leak.

High

NHTSAMay 21, 2021Nationwide• RUGGED MOUNTAIN CUSTOM RV

Canon Vantage Galan 3T (Canon) – Flame Retardancy Problem (2021)

Fire/Burn Risk

The MRI system contains a component that does not meet the appropriate flame retardancy-rating which could result in smoke or fire.

High

FDAMay 21, 2021Nationwide• Canon Medical System, USA, INC.

Toshiba Vantage Tiitan 1.5T (Canon) – Flame Retardancy Risk (2021)

Fire/Burn Risk

The MRI system contains a component that does not meet the appropriate flame retardancy-rating which could result in smoke or fire.

High

FDAMay 21, 2021Nationwide• Canon Medical System, USA, INC.