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TECHNO-PATH MANUFACTURING LTD. Fort Henry Business Park Ballina Tipperary Ireland

TECHNO-PATH MANUFACTURING LTD. Fort Henry Business Park Ballina Tipperary Ireland Recalls

All product recalls associated with TECHNO-PATH MANUFACTURING LTD. Fort Henry Business Park Ballina Tipperary Ireland.

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Recall Summary

Total Recalls

1000

Past Year

206

Class I (Serious)

410

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 501–520 of 3552 recalls

Multichem P (Techno-Path) – glass vial commodity problem (2023)

Laceration Risk

Technopath Manufacturing Ltd. has identified an issue with the glass vial commodity used to fill the Multichem S Plus Level 1, Multichem S Plus Level 2, Multichem S Plus Level 3, Multichem IA Plus and Multichem P Controls. Some customers have experienced broken vials when receiving or thawing Technopath Multichem IA Plus and Multichem S Plus Controls. Breakages have been observed upon delivery, while thawing or while opening the vial. The breakages can result in the bottom of the vial breaking off, breakage in the neck thread area or cracking on the sides of the vial. This may expose the user to biohazardous material if cut and may cause a delay in patient results.

Moderate

FDAAug 25, 2023Nationwide• TECHNO-PATH MANUFACTURING LTD. Fort Henry Business Park Ballina Tipperary Ireland

Philips Tempus Pro Monitor (Remote Diagnostic) – screen error issue (2023)

Full screen error message may occur on patient monitors with affected hardware version, either during or after laryngoscopes are unplugged from monitors, informing users a 60-100 second shutdown/restart are required. Error prevents: viewing graphical patient vital signs, sounding of pulse audio tone, visualization of patient airway used during intubation; may lead to treatment delay or hypoxia.

High

FDAAug 24, 2023AL, AZ, CA +39 more

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• Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom

LFS Flat Screen Support Arm (DKK Dai-Ichi) – stopper block issue (2023)

The stopper block on the LFS bracket could be broken or missing. Without this stopper block, the flat screen attached to the LFS flat screen system can rotate beyond the original angle limit and it could cause excessive force to be given to the spring shaft of the LFS bracket. Due to the excessive force given to the spring shaft, the spring shaft could break and shear off.

High

FDAAug 23, 2023MI• DKK Dai-Ichi Shomei Co., Ltd. 1 Chome 32-26 Sakashita Itabashi Japan

LFS Flat Screen Arm (DKK Dai-Ichi) – stopper block issue (2023)

High

FDAAug 23, 2023MI• DKK Dai-Ichi Shomei Co., Ltd. 1 Chome 32-26 Sakashita Itabashi Japan

3M Attest Biological Indicator (3M) – Multiple Lot Defects (2023)

Specific lots of 3M Attest Super Rapid Readout Biological Indicators (1492V), 3M Attest Super Rapid 5 Steam-Plus Challenge (41482V, 41482VF), and 3M Attest Super Rapid Readout Steam Challenge (1496V) may contain biological indicators with a cap that melts, deforms and/or cracks following a steam sterilization cycle of 132C and 135C.

Moderate

FDAAug 22, 2023Nationwide• 3M Company Health Care Business 3m Center

3M Attest Steam Challenge Pack (3M) – Multiple Lot Defects (2023)

Moderate

FDAAug 22, 2023Nationwide• 3M Company Health Care Business 3m Center

Toddler Towers (Simplay3) – Fall and Injury Risk (2023)

This recall involves Simplay3 Toddler Towers with model 41807. The towers were sold in a variety of colors including espresso, white and gray. The name Simplay3 is printed on the base of the tower and along the upper railing of the tower. The product's dimensions are 34" x 17.5" x 16". The model number is printed on the base of the tower. Model Date Codes 41807-01 (espresso) Nov 2018- June 2023 41807-02 (gray) Nov 2018- June 2023 41807-03 (white) Nov 2018- June 2023

High

CPSCAug 17, 2023Nationwide• The Simplay3 Company, of Streetsboro, Ohio

Exoplan Software (Exocad) – Export Filtering Error (2023)

A software library filtering error has been discovered which occurs when users are using the Step-by-Step Full Drill Protocol export functionality of exoplan 3.1 Rijeka. When a guided surgery treatment approach is selected, along with a Step-by-Step Full Drill Protocol export implant library, exoplan software does not filter out unsupported sleeve height positions for a particular sub-full drill protocol and instead shows ALL possible sleeve height positions for all sub-full drill protocols. The use of an improper sleeve height position in a surgical guide could result in patient injury

High

FDAAug 17, 2023Nationwide• Exocad GmbH Julius-Reiber-Str. 37 Darmstadt Germany

Philips Allura Xper (Philips) – Foot Switch Damage (2023)

A damaged foot switch may cause instances where no or only intermittent x-ray radiation initiation is possible.

Moderate

FDAAug 15, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Seafood Crabmeat Stuffing (Shaw's) – Plastic Fragment (2023)

A piece of brittle plastic was found in seafood crabmeat stuffing mix.

Class IIModerate

FDAAug 14, 2023Nationwide• Shaw's Southern Belle Frozen Foods, Inc.

Avent Baby Monitors (Philips) – Burn risk (2023)

Fire/Burn Risk

This recall involves Philips Avent video baby monitors used to remotely monitor infants. They consist of a Baby Unit (camera) and a Parent Unit (monitor) pair. The monitor has a 3.5-inch color screen. The recalled baby monitors include models SCD630 and SCD843 only, manufactured between March 2016 and December 2019. The model numbers and production date codes, in day-month-year format, are located on the bottom of the Parent Unit. The monitors and camera are white. Philips Avent is printed on the front.

High

CPSCAug 3, 2023Nationwide• Philips Consumer Lifestyle B.V., of The Netherlands

Henke-Ject-2 Syringes (Wolf) – sterile barrier damage (2023)

Sterile barrier might be damaged compromising the sterility of the device.

Moderate

FDAJul 27, 2023Nationwide• Wolf, Henke Sass, Gmbh Kronenstrasse 16 Tuttlingen Germany

Peanut Butter Taffy (Mehlenbacher's) – Undeclared Milk (2023)

Undeclared Allergen

Undeclared allergen; milk

Class IIModerate

FDAJul 20, 2023Nationwide• Mehlenbacher's Taffy

Strawberry Taffy (Mehlenbacher's) – Undeclared Milk (2023)

Undeclared Allergen

Undeclared allergen; milk

Class IIModerate

FDAJul 20, 2023Nationwide• Mehlenbacher's Taffy

Zenition 70 (Philips) – Radiation Exposure Risk (2023)

Philips has become aware of the potential for unintended radiation exposure with Zenition 70 systems with Vascular Extension option and a Wireless Foot Switch.

Moderate

FDAJul 20, 2023Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands