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Cellavision AB Forskningsbyn Ideon Scheelevagen 19a Lund Sweden

Cellavision AB Forskningsbyn Ideon Scheelevagen 19a Lund Sweden Recalls

All product recalls associated with Cellavision AB Forskningsbyn Ideon Scheelevagen 19a Lund Sweden.

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Recall Summary

Total Recalls

1000

Past Year

169

Class I (Serious)

125

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 101–120 of 1553 recalls

Digital Cell Morphology Analyzer (Cellavision) – Barcode Reading Error (2025)

Automated cell-locating device barcode reader may read the barcode of the previously processed slide resulting in a misattribution of diagnostic results.

Moderate

FDAOct 8, 2025Nationwide• Cellavision AB Forskningsbyn Ideon Scheelevagen 19a Lund Sweden

BMW X5 (BMW) – Starter Assembly Problem (2025)

Fire/Burn Risk

BMW of North America, LLC (BMW) is recalling certain 2020 340I, X6, 2020-2025 840I, 2020-2022 740LI, 2019-2020 X7, and X5 vehicles. After repeated attempts, the starter motor may overheat from an electrical overload.

NHTSASep 25, 2025Nationwide• BMW

BMW M4 (BMW) – Battery Cable Connection Fault (2025)

Fire/Burn Risk

BMW of North America, LLC (BMW) is recalling certain 2026 M4 and 430i vehicles. The positive battery cables may not be properly connected to the power distribution box, resulting in an engine stall and a fire.

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High

NHTSASep 25, 2025Nationwide• BMW

BMW 530i (BMW) – Starter Relay Issue (2025)

Fire/Burn Risk

BMW of North America, LLC (BMW) is recalling certain 2019-2021 BMW 330i, 2019-2022 BMW Z4, 2020-2022 BMW 530i, X3, X4, Toyota Supra, 2021-2022 BMW 430i, 430i Convertible, and 2022 BMW 230i vehicles. The engine starter relay may corrode, causing the relay to overheat and short circuit.

NHTSASep 23, 2025Nationwide• BMW

AR-15 Chamber Lock Pro (StopBox USA) – Serious Injury Risk (2025)

Fire/Burn Risk

This recall involves certain AR-15 Chamber Lock Pro firearm locks shipped between June 2 and July 15, 2025. Consumers can find their shipping date by contacting StopBox by phone, email, or online at https://stopboxusa.com/pages/stopbox-ar-15-chamber-lock-recall. This is a device designed to lock into the chamber of an AR-15 style rifle and prevent it from firing. The product is made of anodized aluminum machined parts, was sold in red and black, and has five buttons that correspond to each finger. It has the StopBox "S" logo and "CHAMBER LOCK PRO AR-15" laser etched on the back of the product.

CPSCSep 4, 2025Nationwide• StopBox USA, of Spokane Valley, Washington

BMW X5 Plug-In Hybrid (BMW) – Windshield Fasteners (2025)

Fire/Burn Risk

BMW of North America, LLC (BMW) is recalling certain 2026 X5 Plug-in Hybrid, X5, and X7 vehicles. The windshield may not be sealed properly, which can allow water to enter the power distribution box or electronic control unit.

NHTSAAug 27, 2025Nationwide• BMW

Venclose digiRF Generator (Bard) – Wiring Detection Feature (2025)

Laceration Risk

Software version 3.35 of the Venclose digiRF Generator incorporates a catheter verification feature specifically designed to detect internal wiring anomalies in Venclose EVSRF Ablation Catheters prior to clinical use. This automated diagnostic check is executed immediately upon catheter connection to the generator, occurring before the procedure interface becomes accessible. When a catheter fails this verification process, the generator displays a Red X indicator on the screen without accompanying error codes, effectively disabling catheter functionality. However, BD has determined that software version 3.35 generates false positive failures due to temperature-dependent verification parameters, incorrectly flagging properly functioning Venclose EVSRF Ablation Catheters as defective when the catheter temperature is not at steady state during the check initiation.

FDAAug 21, 2025Nationwide• Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438

RayStation Software (RaySearch) – UID uniqueness (2025)

DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.

FDAAug 8, 2025Nationwide• RAYSEARCH LABORATORIES AB Eugeniavagen 18c Stockholm Sweden

Argus PB-3000 Monitor (Schiller) – measurement error (2025)

Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.

FDAAug 8, 2025Nationwide• Schiller, Ag Altgasse 68 Baar Switzerland

Ortoma Inserter Adapter (Ortoma) – weld breakage (2025)

Due to a weld breakage between the pin and inserter holder of the Inserter Adapter.

FDAJul 28, 2025Nationwide• ORTOMA AB Falkenbergsgatan 3 Goteborg Sweden

BMW S 1000 R (BMW) – Crash Notification Error (2025)

BMW of North America, LLC (BMW) is recalling certain 2025 F 900 GS, F 800 GS, R 1300 GS Adventure, R 1300 GS, S 1000 RR, S 1000 R, and K 1600 GT vehicles equipped with the optional emergency call system. The emergency call system (eCall) may have been deactivated due to a software programming error.

NHTSAJul 25, 2025Nationwide• BMW

BMW I5 (BMW) – Electric Motor Software Issue (2025)

BMW of North America, LLC (BMW) is recalling certain 2022-2025 i4, 2022-2024 IX, 2023-2024 I7, and 2024 I5 vehicles. The electric drive motor software may shut down the high-voltage system, causing a loss of drive power.

NHTSAJul 23, 2025Nationwide• BMW

BMW I4 (BMW) – Battery Cell Issue (2025)

Fire/Burn Risk

BMW of North America, LLC (BMW) is recalling certain 2022-2025 IX, 2023-2024 I7, and 2022-2023 i4 vehicles. The high-voltage battery cell modules may not have been assembled properly, resulting in stress on the module frame and possible module failure.

NHTSAJul 16, 2025Nationwide• BMW

3mensio Workstation (PIE Medical) – Measurement Error (2025)

When fenestrated analysis with clock measurements is started in diagnostic bioimaging software (intended to measure/visualize cardiovascular structures) and the 12h position of a single clock is changed, other clock measurements are not updated relative to the new 12h position which may cause stent graft fenestrations at incorrect position, which may lead to blood flow disruption and tissue damage

FDAJul 14, 2025Nationwide• PIE Medical Imaging B.V. Demertdwarsstraat 8A01 Maastricht Netherlands

Semaglutide Injection 4mL (Boothwyn Pharmacy) – Subpotent Drug (2025)

Subpotent Drug

Class IIModerate

FDAJul 9, 2025Nationwide• Boothwyn Pharmacy LLC

Semaglutide Injection (Boothwyn Pharmacy) – Subpotent Drug (2025)

Subpotent Drug

Class IIModerate

FDAJul 9, 2025Nationwide• Boothwyn Pharmacy LLC

Semaglutide Injection (Boothwyn Pharmacy) – Potency Issue (2025)

Subpotent Drug

Class IIModerate

FDAJul 9, 2025Nationwide• Boothwyn Pharmacy LLC

Fluorescein 2% Ophth (Boothwyn Pharmacy) – Subpotent Drug (2025)

Subpotent Drug

Class IIILow

FDAJul 9, 2025Nationwide• Boothwyn Pharmacy LLC

Endless Highways (BOWLUS) – Manual Issue (2025)

Bowlus Road Chief LLC (Bowlus) is recalling certain 2022-2023, 2025 Endless Highways, 2024-2025 Volterra, 2024 Terra Firma, and 2025 Rivet trailers equipped with an elongated hitch. The owners manual does not include instructions to retighten the two hitch bolts in the maintenance schedule.

NHTSAJun 27, 2025Nationwide• BOWLUS

LiPRO Battery Packs (DR Power) – fire hazard (2025)

Fire/Burn Risk

This recall involves 62-volt 5.0 Ah LiPRO rechargeable lithium-ion battery packs for use with DR Power brand battery-powered products, such as lawnmowers, trimmers and snow throwers. The products include stand-alone battery packs with model number 414240, and removeable battery packs included with DR Power outdoor yard equipment items with model numbers 524340, SB11022XEN, T4X3026XEN, T4X3062XENR, CE75021XEN0 and CE77021XEN0. Information containing the model number for the battery pack ("41424") is located on the battery pack's label. The LiPRO and DR Power logo are on the front and side panels of the battery pack. Note: Do not throw this recalled lithium-ion battery or device in the trash, the general recycling stream (e.g., street-level or curbside recycling bins), or used battery recycling boxes found at various retail and home improvement stores. Recalled lithium-ion batteries must be disposed of differently than other batteries, because they present a greater risk of fire. Your municipal household hazardous waste (HHW) collection center may accept this recalled lithium-ion battery or device for disposal. Before taking your battery or device to a HHW collection center, contact that office ahead of time and ask whether it accepts recalled lithium-ion batteries. If it does not, contact your municipality for further guidance.

CPSCJun 26, 2025Nationwide• Ningbo New Team Import & Export Co. Ltd. ("Lera"), of China