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Augmedics Ltd. 2 Ha-Otsma St Yokneam Illit Northern Israel

Augmedics Ltd. 2 Ha-Otsma St Yokneam Illit Northern Israel Recalls

All product recalls associated with Augmedics Ltd. 2 Ha-Otsma St Yokneam Illit Northern Israel.

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Recall Summary

Total Recalls

624

Past Year

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 41–60 of 624 recalls

Augmedics Perc Pin Adaptor (Augmedics) – Tightening Marking (2025)

The perc pin adaptor AMCH07200 tightening knob was found to be inconvenient to the user and the tightening markings found to be improperly placed.

Moderate

FDAApr 14, 2025Nationwide• Augmedics Ltd. 2 Ha-Otsma St Yokneam Illit Northern Israel

PiezoWave 2 Control Unit (Richard Wolf) – Capacitor Failure (2025)

Fire/Burn Risk

The high voltage capacitor may fail early in the product life cycle after delivery of surge voltages. When this failure occurs, the capacitor may produce smoke and a burning smell. In extremely rare instances a capacitor may cause a spark or excessive heat when an internal capacitor failure occurs.

High

FDAApr 9, 2025GA• Richard Wolf GmbH Pforzheimer Str. 32 Knittlingen Germany

KliniTray Tissue Margin Board (Klinika Medical) – Microbial Contamination (2025)

Potential for microbial contamination.

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Moderate

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

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

Potential for microbial contamination.

Low

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

Distal Femoral Augment (Waldemar Link) – Missing Thread Screw (2025)

The device was delivered with a preassembled Femoral Augment screw that was missing its thread.

Low

FDAApr 3, 2025Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Tibial Augment (Waldemar Link) – Missing Thread Screw (2025)

The device was delivered with a preassembled Femoral Augment screw that was missing its thread.

Low

FDAApr 3, 2025Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

L-Shaped Femoral Augment (Waldemar Link) – Missing Thread Screw (2025)

The device was delivered with a preassembled Femoral Augment screw that was missing its thread.

Low

FDAApr 3, 2025Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Posterior Femoral Augment (Waldemar Link) – Missing Thread Screw (2025)

The device was delivered with a preassembled Femoral Augment screw that was missing its thread.

Low

FDAApr 3, 2025Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

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.

Moderate

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

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.

Moderate

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.

Moderate

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

DORO Easy-Connect Navigator (Pro-Med) – reference array issue (2025)

Potential of compromised compatibility resulting in influence on the positioning of the reference array and an influence of the function of the navigation system cannot be excluded.

Moderate

FDAMar 14, 2025Nationwide• Pro-Med Instruments Gmbh BOETZINGER STRASSE 86 Freiburg Im Breisgau Germany

Gerolsteiner Sparkling Water (Gerolsteiner) – Laceration Hazard (2025)

Laceration Risk

This recall involves Gerolsteiner 750ml sparkling water bottles from two specific lots. The water was sold in large 750ml glass bottles or in cases containing 15 bottles. There is a white, blue and red label on the front of the bottle with the name "Gerolsteiner". The lot number is located on the lower part of the label. Affected bottles have a lot number 11/28/2024 L or 11/27/2024 L.

Moderate

CPSCMar 13, 2025Nationwide• Gerolsteiner Brunnen GmbH & Co. KG, of Germany

Modular Stem (Waldemar Link) – Carton Label Error (2025)

A problem was discovered during the scanning process of the outer carton label because of an incorrect GTIN on the label, which is a GTIN for a different product.

Low

FDAFeb 14, 2025Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

GMC Savana (GMC) – Door Impact Beam Issue (2025)

General Motors LLC (GM) is recalling certain 2025 Chevrolet Express and GMC Savana vans. The impact beam located in the driver's side door may have improper welds.

High

NHTSAFeb 13, 2025Nationwide• GMC

GMC Sierra 1500 (GMC) – grille deflector attachment (2025)

General Motors, LLC (GM) is recalling certain 2022 GMC Sierra 1500 vehicles equipped with chrome front grille deflectors. The attachments that hold the front grille deflectors in place may fracture, resulting in grille detachment.

Moderate

NHTSAFeb 6, 2025Nationwide• GMC

Leica CM1950 Cryostat (Leica) – firmware data loss (2025)

Firm became aware of software issues related to most recent firmware update which could result in loss of patient tissue.

High

FDAJan 30, 2025Nationwide• LEICA BIOSYSTEMS NUSSLOCH GMBH Heidelberger Str. 17-19 Nussloch Germany

GMC Sierra EV (GMC) – rear seat belt anchorage (2025)

General Motors, LLC (GM) is recalling certain 2024 Chevrolet Silverado EV and 2024-2025 GMC Sierra EV pickup trucks. The bolt that secures the rear center seat belt assembly to the seat structure may not have been properly tightened.

High

NHTSAJan 16, 2025Nationwide• GMC

MSOT Acuity Echo (Ithera) – Safety Instruction (2025)

The MSOT Acuity Echo does not include an adequate instruction for safe operation of the device. The previous version of the user manuals contained a wrong value for the Nominal Ocular Hazard Distance (NOHD).

Moderate

FDAJan 8, 2025Nationwide• Ithera Medical Gmbh Zielstattstr. 13 Munich Germany

CryoSolutions Cartridges (New Medical Technologies) – Valve Premature Opening (2024)

During the assembly of the cartridge to its connecting body part, the valve may open prematurely resulting in partial or complete emptying of the cartridge before its intended use.

Moderate

FDADec 19, 2024Nationwide• New Medical Technologies Gmbh Wankdorffeldstrasse