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Ansell Healthcare Products LLC

Ansell Healthcare Products LLC Recalls

All product recalls associated with Ansell Healthcare Products LLC.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 5501–5520 of 37665 recalls

Gammex Non-Latex PI Green Surgical Gloves (Ansell) – pouch seal issue (2023)

Some surgical glove sterile pouches were not completely sealed.

Moderate

FDAAug 3, 2023Nationwide• Ansell Healthcare Products LLC

Novaplus Gammex Non-Latex PI Green Surgical Gloves (Ansell) – pouch seal issue (2023)

Some surgical glove sterile pouches were not completely sealed.

Moderate

FDAAug 3, 2023Nationwide• Ansell Healthcare Products LLC

ReNewal Ligasure Maryland Jaw Sealer (MEDLINE) – packaging seal issue (2023)

Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray.

Low

FDAAug 3, 2023Nationwide

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Page 276 of 1884Next

• MEDLINE INDUSTRIES, LP Northfield

ReNewal Ligasure Blunt Tip Sealer (MEDLINE) – packaging seal issue (2023)

Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray.

Low

FDAAug 3, 2023Nationwide• MEDLINE INDUSTRIES, LP Northfield

EU7000is Portable Generators (Honda) – Fire risk (2023)

Fire/Burn Risk

This recall involves Honda Portable Generators with model number EU7000is. They are red and gray in color and measure about 33 inches long, 28 inches wide and 28 inches high. Honda and EU7000is are printed on the side of the generator. The following serial numbers are included in this recall: EEJD-1364963 through EEJD-1366026. The serial number decal is located inside the access door.

High

CPSCAug 3, 2023Nationwide• American Honda Motor Co. Inc., of Torrance, California

3T Heater Cooler System (LivaNova) – maintenance schedule error (2023)

The firm's labeling (Quick Reference Guide) contains incorrect information in the maintenance schedule for the Heater-Cooler device.

Low

FDAAug 3, 2023Nationwide• LivaNova Deutschland GmbH Lindberghstr. 25 Munich Germany

Sterile Iris Scissors (MEDLINE) – tip protector risk (2023)

4.5" Iris Scissors, Sterile, Curved (DYNJ04049) are being recalled due to the potential of the tip protector to fall off. The sharp tip of the scissors could compromise the sterile barrier system by puncturing large and/or small holes that may not be visible to the user.

Moderate

FDAAug 3, 2023Nationwide• MEDLINE INDUSTRIES, LP Northfield

Liquid Assayed Chemistry Control (Randox) – instructions error (2023)

there has been a transcription error in the Instructions for Use (IFU) for the Liquid Assayed Chemistry Control Premium Plus Level 3. For Caeruloplasmin, the one and two standard deviation values printed on the sheet are incorrect, which may lead to misreporting patient results. Target and range values are correct, and risk is mitigated; most clinical labs will use the target and range values in clinical practice.

Moderate

FDAAug 3, 2023GA, OH, OR +3 more• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

ReNewal Harmonic ACE+7 Shears (MEDLINE) – packaging seal issue (2023)

Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray.

Low

FDAAug 3, 2023Nationwide• MEDLINE INDUSTRIES, LP Northfield

Utilimaster Upfit (UTILIMASTER) – battery cable issue (2023)

Fire/Burn Risk

Shyft Group is recalling certain 2023 Utilimaster Upfit vehicles. The battery cable connections for the electrical harness may be connected incorrectly, causing the circuit protection on the cables to be ineffective.

High

NHTSAAug 2, 2023Nationwide• UTILIMASTER

Incisive CT (Philips) – software compliance concerns (2023)

Philips has identified three software issues with compliance concerns to Subchapter J: Issue 1: Coronary Computed Tomography Angiography (CTA) scan may not be triggered at the optimal time. Issue 2: Use of aborted surview for scan planning will result in deviation from intended scan area. Issue 3: Actual clinical scan with bariatric (Noah) couch will deviate from the intended scan area if surview scan length is greater than 1832mm.

Moderate

FDAAug 2, 2023Nationwide• Philips Healthcare

Translead Dry Van Trailer (HYUNDAI) – steering problem (2023)

Hyundai Translead is recalling certain 2022 V/T 53SW Q29485 VI2530154-AFJ Dry Van trailers equipped with Dexter Smart-Steer 2.0 Axles with bolt-on steering arms. The steering arm may fracture during certain conditions, such as low speed and high side-loading.

High

NHTSAAug 2, 2023Nationwide• HYUNDAI TRANSLEAD