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Klinika Mdical Gmb Achtzehnmorgenweg 6 Usingen Germany

Klinika Mdical Gmb Achtzehnmorgenweg 6 Usingen Germany Recalls

All product recalls associated with Klinika Mdical Gmb Achtzehnmorgenweg 6 Usingen Germany.

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Recall Summary

Total Recalls

1000

Past Year

567

Class I (Serious)

25

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 441–460 of 7756 recalls

KliniTray Faxitron Plate (Klinika Medical) – Microbial Contamination (2025)

Potential for microbial contamination.

FDAApr 4, 2025Nationwide• Klinika Mdical Gmb Achtzehnmorgenweg 6 Usingen Germany

Casement Window Hinge Tracks (AmesburyTruth) – Impact Injury (2025)

This recall involves Ashland 10-inch and 14-inch two-bar right-hand and left-hand casement window hinge tracks installed in windows to allow the windows to be cranked opened and closed. The casement window hinge tracks include part numbers 2003558, 2003559, 2004271 and 2004272. These products can be identified by locating "R10," "L10," "R14" or "L14" located on the face of the casement window hinge track. These hinge tracks were manufactured and sold to residential and commercial window manufacturers in boxes dated April 2024 through December 2024.

CPSCApr 3, 2025Nationwide• Amesbury Industries Inc., d/b/a AmesburyTruth, of Houston, Texas

Aquadis 56 Washer Disinfector (Getinge) – Circulation Pump Timing Error (2025)

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The frequency inverter is not programmed by supplier according to specification which causes the circulation pump to start earlier than expected, resulting in additional wear and tear, earlier than expected, on the axial seal in the pump housing.

FDAApr 2, 2025Nationwide• Getinge Disinfection Ab Ljungadalsgatan

myQA iON (IBA Dosimetry) – Analysis Result Inaccuracy (2025)

Wrong analysis results can occur if the user creates two structures with the same name, except for one differing by a special character.

FDAApr 1, 2025Nationwide• IBA Dosimetry GmbH Bahnhofstr. 5 Schwarzenbruck Germany

Dexmedetomidine HCl (Denver Solutions) – Leaking Syringes (2025)

Lack of Assurance of Sterility: Leaking/damaged syringes.

Class IIModerate

FDAMar 31, 2025Nationwide• Denver Solutions, LLC DBA Leiters Health

Rocuronium Bromide (Denver Solutions) – Leaking Syringes (2025)

Lack of Assurance of Sterility: Leaking/damaged syringes.

Class IIModerate

FDAMar 31, 2025Nationwide• Denver Solutions, LLC DBA Leiters Health

Glycopyrrolate (Denver Solutions) – Leaking Syringes (2025)

Lack of Assurance of Sterility: Leaking/damaged syringes.

Class IIModerate

FDAMar 31, 2025Nationwide• Denver Solutions, LLC DBA Leiters Health

Ketamine HCl (Denver Solutions) – Leaking Syringes (2025)

Lack of Assurance of Sterility: Leaking/damaged syringes.

Class IIModerate

FDAMar 31, 2025Nationwide• Denver Solutions, LLC DBA Leiters Health

Phenylephrine HCl (Denver Solutions) – Leaking Syringes (2025)

Lack of Assurance of Sterility: Leaking/damaged syringes.

Class IIModerate

FDAMar 31, 2025Nationwide• Denver Solutions, LLC DBA Leiters Health

Guide Wire with Ruler Tube (Stryker) – Metal Ring Detachment Risk (2025)

The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.

FDAMar 28, 2025Nationwide• Stryker GmbH Bohnackerweg 1 Selzach Switzerland

Guide Wire with Ruler Tube (Stryker) – Metal Ring Detachment Risk (2025)

The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.

FDAMar 28, 2025Nationwide• Stryker GmbH Bohnackerweg 1 Selzach Switzerland

Walker's Wine Juice Pumpkin Juice (Walker's Fruit Basket) – Botulinum Contamination (2025)

May be contaminated with Clostridium botulinum

FDAMar 28, 2025IL, IN, KS +9 more• Walker's Fruit Basket and Press House

DxI 9000 Access Immunoassay Analyzer (Beckman Coulter) – Host System Connectivity (2025)

When DxI 9000 Access Immunoassay Analyzer is connected to a host system (laboratory information system (LIS) or middleware) and has accumulated canceled QC test results that were not sent by LIS, the analyzer may lose communication with the host system. The lost connection interrupts sample processing, which delays reporting patient test results and may subsequently delay patient treatment.

FDAMar 27, 2025Nationwide• Beckman Coulter, Inc.

Skytron Freedom Monitor Mount (IHB Operations) – Mounting Hardware Risk (2025)

The mounting hardware that is supplied with the 4FXS-60 monitor bracket does not provide adequate thread engagement to support the weight of the frame and monitor. This could lead to a failure of the mounting hardware and subsequent separation of the frame from the mounting column.

FDAMar 27, 2025Nationwide• IHB OPERATIONS B.V. Floresstraat 52 Zwolle Netherlands

Duloxetine Capsules (Breckenridge) – Nitrosamine Impurity (2025)

CGMP Deviations: presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the recommended interim limit.

Class IIModerate

FDAMar 26, 2025Nationwide• Breckenridge Pharmaceutical, Inc.

IceSeed 1.5 CX Needle OUS (Boston Scientific) – Demo Settings Issue (2025)

Laceration Risk

Boston Scientific has identified that IceSeedTM CX needles manufactured between April 2024 and February 2025 have been programmed with DEMO settings instead of Commercial settings (see Affected Product Listing). Upon initial connection of an IceSeed CX needle to the Cryoablation System, the user will be prompted to perform the Needle Integrity and Functionality Test (NIT) per standard protocols. The affected needles perform as intended unless they are disconnected and reconnected to any channel after testing. In this case, the Cryoablation System will prompt re-execution of the NIT.

FDAMar 24, 2025Nationwide• Boston Scientific Corporation

IceSeed 1.5 CX S Needle OUS (Boston Scientific) – Demo Settings Issue (2025)

Laceration Risk

Boston Scientific has identified that IceSeedTM CX needles manufactured between April 2024 and February 2025 have been programmed with DEMO settings instead of Commercial settings (see Affected Product Listing). Upon initial connection of an IceSeed CX needle to the Cryoablation System, the user will be prompted to perform the Needle Integrity and Functionality Test (NIT) per standard protocols. The affected needles perform as intended unless they are disconnected and reconnected to any channel after testing. In this case, the Cryoablation System will prompt re-execution of the NIT.

FDAMar 24, 2025Nationwide• Boston Scientific Corporation

IceSeed 1.5 CX S Needle US (Boston Scientific) – Demo Settings Issue (2025)

Laceration Risk

Boston Scientific has identified that IceSeedTM CX needles manufactured between April 2024 and February 2025 have been programmed with DEMO settings instead of Commercial settings (see Affected Product Listing). Upon initial connection of an IceSeed CX needle to the Cryoablation System, the user will be prompted to perform the Needle Integrity and Functionality Test (NIT) per standard protocols. The affected needles perform as intended unless they are disconnected and reconnected to any channel after testing. In this case, the Cryoablation System will prompt re-execution of the NIT.

FDAMar 24, 2025Nationwide• Boston Scientific Corporation

IceSeed 1.5 CX Needle US (Boston Scientific) – Demo Settings Issue (2025)

Laceration Risk

Boston Scientific has identified that IceSeedTM CX needles manufactured between April 2024 and February 2025 have been programmed with DEMO settings instead of Commercial settings (see Affected Product Listing). Upon initial connection of an IceSeed CX needle to the Cryoablation System, the user will be prompted to perform the Needle Integrity and Functionality Test (NIT) per standard protocols. The affected needles perform as intended unless they are disconnected and reconnected to any channel after testing. In this case, the Cryoablation System will prompt re-execution of the NIT.

FDAMar 24, 2025Nationwide• Boston Scientific Corporation

Connex Vital Signs Monitor (Baxter) – Battery Fire Risk (2025)

There were customer reports of devices which experienced battery-related fires. The investigation found that the devices in question were utilizing third-party, after-market batteries that are not approved by Baxter.

FDAMar 24, 2025Nationwide• Baxter Healthcare Corporation