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Kawasaki Motors Manufacturing Corp. U.S.A. (engine manufacturer), of Maryville, Missouri

Kawasaki Motors Manufacturing Corp. U.S.A. (engine manufacturer), of Maryville, Missouri Recalls

All product recalls associated with Kawasaki Motors Manufacturing Corp. U.S.A. (engine manufacturer), of Maryville, Missouri.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 1441–1460 of 25000 recalls

John Deere ZTrak Mowers (Kawasaki) – Fire Hazard (2025)

Fire/Burn Risk

This recall involves John Deere ZTrak Zero Turn Mowers with model numbers Z720E, Z730M, Z740R and Z760R with Kawasaki engines. Model Start Serial Number End Serial Number Z720E 1TC720E****010001 1TC720E****080657 Z730M 1TC730M****010001 1TC730M****080574 Z740R 1TC740R****010001 1TC740R****080462 Z760R 1TC760R****080001 1TC760R****080339

High

CPSCJan 2, 2025Nationwide• Kawasaki Motors Manufacturing Corp. U.S.A. (engine manufacturer), of Maryville, Missouri

Duloxetine Capsules 30mg (Rising Pharma) – CGMP impurity risk (2024)

CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended interim limit.

Class IIModerate

FDADec 30, 2024Nationwide• Rising Pharma Holding, Inc.

Metformin ER Tablets 500mg (Granules) – foreign tablet found (2024)

1...71 727374 75...1250

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Presence of Foreign Tablets/Capsules: A Paracetamol 500 mg tablet was found in a 1000-count bottle of Metformin HCL ER Tablets USP, 500 mg.

Class IIModerate

FDADec 30, 2024IN, OH• Granules Pharmaceuticals Inc.

Duloxetine Capsules 20mg (Rising Pharma) – CGMP impurity risk (2024)

CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended interim limit.

Class IIModerate

FDADec 30, 2024Nationwide• Rising Pharma Holding, Inc.

Duloxetine Capsules 60mg (Rising Pharma) – CGMP impurity risk (2024)

CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended interim limit.

Class IIModerate

FDADec 30, 2024Nationwide• Rising Pharma Holding, Inc.

NeiMed NasoGel (Neilmed) – Spray Stability Failure (2024)

Due to nasal spray stability failure for bioburden.

High

FDADec 28, 2024Nationwide• Neilmed Pharmaceuticals Inc

Inclusive Orbit Merry-Go-Round (Playdale) – Crush Hazard (2024)

This recall involves the Inclusive Orbit, a spinning play component, similar to a merry-go-round, for playgrounds. The product has three handrails and a seat, and it is designed for a capacity of six children. The platform surface is flush with the ground surrounding it. Recalled model numbers include 560-0042 or 560-0051. Owners of the equipment can contact BCI Burke to determine which unit they have.

High

CPSCDec 26, 2024Nationwide• Playdale Playgrounds LTD, of United Kingdom

Lev5 Susceptibility Discs (Oxoid) – Mislabeling Risk (2024)

Mislabeling; Levofloxacin Antimicrobial susceptibility disc packaging may contain Norfloxacin Antimicrobial Susceptibility discs.

Low

FDADec 23, 2024CA, FL, MA +4 more• Oxoid Limited Wade Road Basingstoke United Kingdom

Astagraf XL 0.5mg (Astellas) – empty capsules risk (2024)

Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain empty capsules

Class IHigh

FDADec 23, 2024Nationwide• Astellas Pharma US Inc.

Prograf 0.5mg (Astellas) – empty capsules risk (2024)

Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain empty capsules

Class IHigh

FDADec 23, 2024Nationwide• Astellas Pharma US Inc.

Smart Drive MX2+ SpeedControl Dial (Max Mobility) – Circuit Board Fault (2024)

Due to faulty circuit board in speed control remote use in conjunction with a wheelchair power assist, their is a potential for lost of control of device potentially resulting in minor and major injuries.

Moderate

FDADec 20, 2024AL, AK, AZ +49 more• Max Mobility LLC

Lipoprotein (a) Test (Randox) – 510(k) Compliance Issue (2024)

Lipoprotein (a) on Roche Cobas c501 with nmol/l claims does not have a 510(k) or PMA.

Moderate

FDADec 20, 2024Nationwide• Randox Laboratories, Limited Ardmore; 55 The Diamond Road Crumlin United Kingdom

Levothyroxine Tablets 75mcg (Lupin) – impurity specification (2024)

Failed Impurities/Degradation Specifications: Out of specifications result observed in the drug substance for impurity test during 3-month long term stability study.

Class IIModerate

FDADec 20, 2024IN, OH• Lupin Pharmaceuticals Inc.

Alfa Romeo Stelvio (Alfa Romeo) – Brake Pedal Fastener Problem (2024)

Chrysler (FCA US, LLC) is recalling certain 2019-2020 Alfa Romeo Giulia and Alfa Romeo Stelvio vehicles. The fastener that connects the brake pedal and the brake booster may have been improperly assembled during manufacturing, which can cause the brake pedal to detach from the brake booster.

Moderate

NHTSADec 19, 2024Nationwide• ALFA ROMEO

RAM 1500 (RAM) – Headlight Module Software Issue (2024)

Chrysler (FCA US, LLC) is recalling certain 2025 Ram 1500 pickup trucks. Incorrect headlight module software may cause the headlights to become inoperative. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices, and Associated Equipment."

Moderate

NHTSADec 19, 2024Nationwide• RAM

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

Lamborghini Revuelto (Lamborghini) – Oil Circuit Screw Defect (2024)

Fire/Burn Risk

Lamborghini (Automobili Lamborghini) is recalling certain 2024 Revuelto vehicles. The oil circuit connection flange screws may have been improperly tightened during assembly, which could cause the oil line to leak.

High

NHTSADec 19, 2024Nationwide• LAMBORGHINI

Bodor P and C Series Laser Machines (Jinan Bodor) – Non-Compliant Lasers (2024)

Non-compliant laser products

Moderate

FDADec 19, 2024Nationwide• Jinan Bodor Cnc Machine Co Ltd NO.1299, XINLUO AVE HI-TECH ZONE Jinan China

Methadone Tablets 5mg (West-Ward) – illegible identification (2024)

Failed Tablet/Capsule Specifications: Illegible product identification for the unit dose configuration only.

Class IIILow

FDADec 19, 2024Nationwide• West-Ward Columbus Inc

GE Healthcare Discovery NM 630 (GE Medical Systems) – Nuclear Medicine System Issue (2024)

GE HealthCare has become aware that certain Infinia, VariCam/VG/VH, Brivo NM 615, Discovery NM 630, Discovery NM/CT 670, and Optima NM/CT 640 Nuclear Medicine systems (see Affected Products Details and Appendices) could have been transported or relocated without proper detector support, which can result in excessive load being applied to the detector mounting mechanisms. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

High

FDADec 18, 2024Nationwide• GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING 4, Hayozma St Tirat Carmel Israel