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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

591

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 3441–3460 of 10393 recalls

RayStation (RaySearch) - Incorrect Beam Positioning (2021)

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

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

Ketamine HCl Injection (Prisma Health) - Incorrect Expiration Date (2021)

Labeling: Incorrect Exp. Date: Incorrect BUD.

Class IIILow

FDAJun 8, 2021IN, SC• Prisma Health Outsourcing Facility

Mephyton (Bausch) - Impurity Specification Failure (2021)

Failed Impurities/Degradation Specifications

Class IIILow

FDAJun 8, 2021

1...171 172173174 175...520

Page 173 of 520Next

Nationwide

• Bausch Health Companies, Inc.

Phytonadione Tablets (Bausch) - Impurity Specification Failure (2021)

Failed Impurities/Degradation Specifications

Class IIILow

FDAJun 8, 2021Nationwide• Bausch Health Companies, Inc.

Platinum (Coach House) - Stove Valve Securing Bolt Issue (2021)

Fire/Burn Risk

Coach House, Inc. (Coach House) is recalling certain 2021 Platinum vehicles 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.

NHTSAJun 7, 2021Nationwide• COACH HOUSE

SIGNA PET/MR (GE Healthcare) - Patient Orientation Button Error (2021)

GE Healthcare has recently become aware of an issue on the affected products listed below where the "Patient Orientation" button may inadvertently be clicked when intending to click on the "Save RX" button. This changes the prescribed patient orientation on the system prior to running the initial 3-Plane Localizer Scan (See Figure 1 for reference to buttons.) Selecting and saving a patient orientation that does not match the patient's actual position may result in incorrectly annotated and/or flipped images.

FDAJun 4, 2021Nationwide• GE Healthcare, LLC

SIGNA Voyager (GE Healthcare) - Patient Orientation Button Error (2021)

FDAJun 4, 2021Nationwide• GE Healthcare, LLC

SIGNA HDxt MR System (GE Healthcare) - Patient Orientation Button Error (2021)

FDAJun 4, 2021Nationwide• GE Healthcare, LLC

SIGNA Creator/Explorer (GE Healthcare) - Patient Orientation Button Error (2021)

FDAJun 4, 2021Nationwide• GE Healthcare, LLC

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.

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

Discovery MR750 3.0T (GE Healthcare) - Patient Orientation Button Error (2021)

FDAJun 4, 2021Nationwide• GE Healthcare, LLC

Discovery MR750w 3.0T (GE Healthcare) - Patient Orientation Button Error (2021)

FDAJun 4, 2021Nationwide• GE Healthcare, LLC

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

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

Spectrum IQ Infusion System (Baxter) - Network Configuration Errors (2021)

System errors were noted following changes the customers implemented to the configuration of their network and server systems. Gateway Server System performance anomalies resulted in excessive Spectrum IQ pump connectivity errors.

FDAJun 4, 2021Nationwide• Baxter Healthcare Corporation

Discovery MR450 1.5T (GE Healthcare) - Patient Orientation Button Error (2021)

FDAJun 4, 2021Nationwide• GE Healthcare, LLC

SIGNA MR380 (GE Healthcare) - Patient Orientation Button Error (2021)

FDAJun 4, 2021Nationwide• GE Healthcare, LLC

Stay Informed

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden Recalls

Recall Summary

RayStation (RaySearch) - Incorrect Beam Positioning (2021)

Ketamine HCl Injection (Prisma Health) - Incorrect Expiration Date (2021)

Mephyton (Bausch) - Impurity Specification Failure (2021)

Phytonadione Tablets (Bausch) - Impurity Specification Failure (2021)

Platinum (Coach House) - Stove Valve Securing Bolt Issue (2021)

SIGNA PET/MR (GE Healthcare) - Patient Orientation Button Error (2021)

SIGNA Voyager (GE Healthcare) - Patient Orientation Button Error (2021)

SIGNA HDxt MR System (GE Healthcare) - Patient Orientation Button Error (2021)

SIGNA Creator/Explorer (GE Healthcare) - Patient Orientation Button Error (2021)

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

Discovery MR750 3.0T (GE Healthcare) - Patient Orientation Button Error (2021)

Discovery MR750w 3.0T (GE Healthcare) - Patient Orientation Button Error (2021)

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

SIGNA Pioneer (GE Healthcare) - Patient Orientation Button Error (2021)

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

SIGNA MR355/MR360 (GE Healthcare) - Patient Orientation Button Error (2021)

Optima MR450w 1.5T (GE Healthcare) - Patient Orientation Button Error (2021)

Spectrum IQ Infusion System (Baxter) - Network Configuration Errors (2021)

Discovery MR450 1.5T (GE Healthcare) - Patient Orientation Button Error (2021)

SIGNA MR380 (GE Healthcare) - Patient Orientation Button Error (2021)