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Hans Kissle Company, LLC

Hans Kissle Company, LLC Recalls

All product recalls associated with Hans Kissle Company, LLC.

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Recall Summary

Total Recalls

1000

Past Year

582

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 1361–1380 of 10937 recalls

Hans Kissle Potato Salad (Hans Kissle) – Undeclared Allergens (2023)

Undeclared Egg

Undeclared egg and soy

Class IIModerate

FDANov 9, 2023CT, MA• Hans Kissle Company, LLC

Buttercream Birthday Cake Ice Cream (Jeni's) – metal pieces (2023)

Potential Foreign Material - aluminum and/or stainless steel pieces

Class IIModerate

FDANov 9, 2023Nationwide• Jeni's Splendid Ice Creams LLC

Tapee Tea (Wiedemann) – undeclared medication (2023)

Samples confirm presence of dexamethasone and piroxicam

Class I

1...67 686970 71...547

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High

FDANov 8, 2023FL, OH• THE WIEDEMANN COMPANY LLC

NIM TriVantage EMG Tube (Medtronic) – Monitoring Issues (2023)

Firm received reports of customers experiencing noise from the NIM System, lead-off or high impedance issues, or loss of/intermittent nerve monitoring,

High

FDANov 7, 2023Nationwide• Medtronic Xomed, Inc.

Medical System (GE) – Bolt Torque Issue (2023)

GE HealthCare has become aware of the potential that incorrect torque has been applied to certain bolts of the Definium Tempo and Definium Tempo Pro products which may result in a potential fall of elements of the Overhead Tube Suspension (OTS) assembly.

High

FDANov 7, 2023Nationwide• GE Hangwei Medical Systems, Co. LTD West Area Bldg. 3, No.1 Yongchang North Road 1 Yongchangbeilu; Beijing Economic and Technological Development Area Beijing China

CARDIOHELP-i System (Maquet) – Factory Settings (2023)

Certain factory settings for the device were incorrectly described in the IFU-related to the warning limits for PVen and PAux, and the default settings for the venous bubble sensor (VBS) and the automatic lock in the Minimized Extracorporeal Circulation (MECC) ThApp

Moderate

FDANov 6, 2023Nationwide• Maquet Medical Systems USA

Fountain Microcatheter (Merit Medical) – sterility risk (2023)

The sterility of microcatheter and infusion system devices cannot be guaranteed.

Very High

FDANov 6, 2023Nationwide• Merit Medical Systems, Inc.

SEROLOGY ToRCH lgM (Randox) – reactivity decrease (2023)

A decrease in the reactivity of HSV Type 1/2 lgM in the Serology ToRCH lgM Positive Control when tested on the DiaSorin Liaison XL.

Moderate

FDANov 6, 2023NY, WV• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Merit Pursue Microcatheter (Merit Medical) – sterility risk (2023)

The sterility of microcatheter and infusion system devices cannot be guaranteed.

Very High

FDANov 6, 2023Nationwide• Merit Medical Systems, Inc.

Merit Maestro Microcatheter (Merit Medical) – sterility risk (2023)

The sterility of microcatheter and infusion system devices cannot be guaranteed.

Moderate

FDANov 6, 2023Nationwide• Merit Medical Systems, Inc.

Allura Systems (Philips) – ceiling mount collision risk (2023)

Ceiling mounted L-arm contains a rotation cover that may potentially be susceptible to falling if a collision between the L-arm and other hospital equipment (i.e., an operating light) were to occur result in injury or potential sterility issues due to the cover becoming loose

Moderate

FDANov 3, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Quantum Biliary Balloon Dilator (Wilson-Cook) – device nonconformity (2023)

Nonconforming devices while manufactured correctly, do not comply to their design requirements. Potential harms associated with balloon detachment are endoscopic retrieval of an impacted or non-impacted object, bleeding caused by the retrieval device, or the incident can occur without injury and the object is left to pass naturally.

Moderate

FDANov 3, 2023Nationwide• Wilson-Cook Medical Inc.

Azurion Systems (Philips) – ceiling mount collision risk (2023)

Moderate

FDANov 3, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Cosco Activity Center – fall hazard (2023)

This recall involves Cosco Jump, Spin & Play Activity Centers with model numbers WA105FZW and WA105GML. The activity centers have a circular hoop base and three poles from which a child seat with a play tray is suspended by three straps. The activity centers are sold in blue and pink, and feature two removable toy animals on the play tray at the front of the seat as well as two toy animals hanging from the front two poles. The activity centers can be adjusted to three different heights.

High

CPSCOct 26, 2023Nationwide• Dorel Juvenile Group Inc., of Columbus, Indiana

Kawasaki Lawn Mower Engines – fire risk (2023)

Fire/Burn Risk

This recall involves Kawasaki engines used in riding lawn mowers sold under the Ariens brand name with mower models IKON, IKON Onyx, and Apex, and under the Gravely brand name with mower models ZT X, ZT XL, ZT HD, and ZT HD Stealth, and under the Husqvarna brand name with mower models TS142TXD, TS242TXD, TS242XD, Z248F, and Z254F, and under the John Deere brand name with mower models Z330M and Z330R, and under the RedMax brand name with mower model RZT48. The recalled engines are model year 2023 FR730V, FR691V, and FR651V. The recalled engine model and serial numbers are located on the engine fan housing. The following model and serial number ranges are included in this recall. Engine Model Number Specification Number FR651V GS28 FR691V GS19 ES29 FR730V FS15 Engine Serial Number Range A full list of serial numbers included in this recall are on the firm's website at www.kawasakienginesusa.com/product-recall.html recall notice RP230415.

High

CPSCOct 26, 2023Nationwide• Kawasaki Motors Manufacturing Corp. U.S.A., of Maryville, Missouri

CD11b APC (BD Biosciences) – cell staining quality (2023)

In vitro diagnostics product that impacts the quality of cell staining can cause low or dim fluorescence signal, which can lead to potential false negative results and misdiagnosis of hematological malignancy, delayed treatment, and the need for additional patient samples.

High

FDAOct 25, 2023Nationwide• Becton, Dickinson and Company, BD Biosciences

INDICAID COVID-19 Test (Phase Scientific) – incorrect expiration (2023)

COVID-19 rapid antigen at home tests were released with an incorrect expiration date of 05 April 2024 when the correct expiration should be 21 February 2024. Expired tests could produce invalid or inaccurate results.

Low

FDAOct 25, 2023Nationwide• PHASE SCIENTIFIC INTERNATIONAL LIMITED 1/f, E Phase 3 Hong Kong Science Park Sha Tin Hong Kong SAR

Nutricia KetcoCal 4:1 LQ Unflavored (Nutricia) – Incorrect Packaging (2023)

Incorrect product in packaging

Class IIModerate

FDAOct 20, 2023AL, CA, CO +18 more• Nutricia North America

RZR Pro XP ROVs (Polaris) – Vehicle Safety Issue (2023)

This recall involves certain VINs of Model Year 2023 RZR PRO XP and PRO XP 4 and Model Year 2024 RZR XP and XP 4 vehicles. The recalled vehicles were sold in the following colors: black, graphite, gray, red and white. The recalled vehicles were sold in two- and four-seat configurations. POLARIS is stamped on the front grille and POLARIS and RZR are printed on the sides of the vehicles. The model name is also printed on the side of the chassis. The VIN is located on the vehicle's frame in the left rear wheel well.

High

CPSCOct 19, 2023Nationwide• Polaris Industries Inc., of Medina, Minnesota

Controller 97745 (Medtronic) – firmware issue (2023)

Units distributed in Korea and Turkey that did not have the correct firmware installed to support the user interface in the local language.

Low

FDAOct 19, 2023Nationwide• Medtronic Neuromodulation