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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

593

Class I (Serious)

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 1501–1520 of 10391 recalls

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

Some surgical glove sterile pouches were not completely sealed.

FDAAug 3, 2023Nationwide• Ansell Healthcare Products LLC

Range Lite Air (HIGHLAND RIDGE) – emergency exit problem (2023)

Highland Ridge RV (Highland Ridge) is recalling certain 2023-2024 Highland Ridge Range Lite Air travel trailers. The trailers may have been manufactured without a secondary emergency exit window.

NHTSAAug 3, 2023Nationwide• HIGHLAND RIDGE

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.

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FDAAug 2, 2023Nationwide• Philips Healthcare

Reusable Distal Attachments (Aomori Olympus) – DEHP risk (2023)

The Distal Attachment contain di-2-ethylhexyl phthalate (DEHP), which exceeds the permissible exposure level calculated according to ISO 10993-17: 2002

FDAJul 27, 2023Nationwide• Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan

Olympus Distal Attachment (Aomori Olympus) – DEHP risk (2023)

The Distal Attachment contain di-2-ethylhexyl phthalate (DEHP), which exceeds the permissible exposure level calculated according to ISO 10993-17: 2002

FDAJul 27, 2023Nationwide• Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan

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

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

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

Sky Wheels (Soft Play) – Fall Hazard (2023)

This recall involves Sky Wheels, which are an individual active play component manufactured for and sold to businesses. They can be incorporated into a larger indoor soft-contained play system. The Sky Wheel is comprised of a 14-inch diameter 4-spoke metal wheel attached to a downward facing milled and threaded shaft which is supported from an overhead bar within the play system framing structure.

CPSCJul 27, 2023Nationwide• Soft Play LLC, of Huntersville, North Carolina

ZVU Functional GI Software (Diversatek) – revision mislabeling (2023)

GI Software labelled as revision 3.3.0 is incorrectly labeled and is in fact revision 3.2.0.

FDAJul 25, 2023Nationwide• Diversatek Healthcare

ADVIA Chemistry Protein Test (Siemens) – reagent carryover (2023)

There is a potential for ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein reagent carryover impacting Enzymatic Creatinine_2 (ECRE_2). Falsely depressed ECRE_2 results may be observed when the assay is processed after the UCFP test on ADVIA Chemistry systems.

FDAJul 25, 2023Nationwide• Siemens Healthcare Diagnostics, Inc.

Trigen Trochanteric Nail (Smith & Nephew) – incorrect implant (2023)

A complaint was received indicating that a package contained a TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 40CM 130 DEGREE LEFT implant instead of a TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 36CM 130 DEGREE LEFT as described on the product label.

FDAJul 24, 2023CA, DE, PA• Smith & Nephew, Inc.

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.

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

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

Undeclared Allergen

Undeclared allergen; milk

Class IIModerate

FDAJul 20, 2023Nationwide• Mehlenbacher's Taffy

Azurion (Philips) – Unintended Radiation Emission (2023)

A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation

FDAJul 19, 2023Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

Allura Xper Series (Philips) – Unintended Radiation Emission (2023)

A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation

FDAJul 19, 2023Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

Freedom Boom Models (IHB) – Suspension Arm Weakness (2023)

Weakened connection point on the adjustable suspension arm, potentially causing damage or a break.

FDAJul 19, 2023AL, AZ, AR +33 more• IHB OPERATIONS B.V. Floresstraat 52 Zwolle Netherlands

MultiDiagnost-Eleva (Philips) – Unintended Radiation Emission (2023)

A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation

FDAJul 19, 2023Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

RayCare Software (RaySearch) – Allergy Warning Issue (2023)

An issue was found in Software RayCare 5A, 5B, 6A, including service packs, where an allergy warning against medication substance (drug ingredient) will not be displayed as expected under certain circumstances

FDAJul 17, 2023Nationwide• RAYSEARCH LABORATORIES AB Eugeniavagen 18c Stockholm Sweden

Frigidaire Gas Laundry Centers (Electrolux) – Fire Hazard (2023)

Fire/Burn Risk

This recall involves all Frigidaire Gas Laundry Centers with model numbers FFLG4033QW and FFLG4033QT. The Laundry Centers were sold in white and titanium colors and have "FRIGIDAIRE" written below the dryer door. The serial number is located on a white sticker inside the dryer door, and the following serial numbers are included in this recall: Model Numbers Serial Numbers FFLG4033QWX 4E44114739 through 4E81603034 FFLG4033QTX 4E44308482 through 4E81603380

CPSCJul 13, 2023Nationwide• Electrolux Home Products Inc., of Charlotte, North Carolina