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Maquet Medical Systems USA

Maquet Medical Systems USA Recalls

All product recalls associated with Maquet Medical Systems USA.

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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 6141–6160 of 37665 recalls

QUADROX-i Neonatal (Maquet) – Packaging Pinhole Risk (2023)

Product packaging may exhibit small pinholes which may not be visible to the unaided eye, compromising the sterile barrier of the packaging. Exposure to non-sterile device may result in inflammation, infection, sepsis, and ischemia.

Very High

FDAMay 18, 2023Nationwide• Maquet Medical Systems USA

Medline Probe Cover Kits (Medline) – Barrier Seam Inadequacy (2023)

Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.

Moderate

FDAMay 18, 2023Nationwide• MEDLINE INDUSTRIES, LP Northfield

Aesculap Surgical Needle (Aesculap) – Product Code Mismatch (2023)

Incorrect product code marked on the product, etched with product code MD611, however; the correct product code is MD610.

Low

1...306 307308309 310...1884

Page 308 of 1884Next

FDA

May 18, 2023

Nationwide

• Aesculap Implant Systems LLC

QUADROX-i Pediatric (Maquet) – Packaging Accessory Damage (2023)

1. An accessory may be improperly placed during packaging, causing creases and damage to the accessory's sterile pouch. 2. Product packaging may exhibit holes, cracks, dents, and crushed areas. Both issues may compromise the sterile barrier of the packaging, and exposure to non-sterile product may result in inflammation, infection, sepsis, and ischemia.

Very High

FDAMay 18, 2023Nationwide• Maquet Medical Systems USA

PhysiciansCare Allergy Tablets (Acme United) – medication issue (2023)

This recall involves PhysiciansCare brand Allergy caplets with item number 90036, Allergy Plus tablets with item number 90091, and Cold and Cough tablets with item numbers 90092 and 90033. They are packaged in boxes of 50, 100 and 250 tablets/caplets. The item numbers are printed on the top right corner of the box. The recall includes the following: Item Number Description 90036 PhysiciansCare Allergy; 50 caplets 90091 PhysiciansCare Allergy Plus; 100 tablets Non-Drowsy Cold and Cough; 100 tablets 90033 PhysiciansCare Cold and Cough; 250 tablets

High

CPSCMay 18, 2023Nationwide• Acme United, of Rocky Mount, North Carolina

Altec Aerial Device (Altec) – Strobe Water Leak (2023)

Fire/Burn Risk

Altec Industries, Inc. (Altec) is recalling certain 2021-2023 Aerial Devices, Digger Derricks, Service Bodies and Cranes. Water can leak into the strobe lights, which could cause an electrical short-circuit.

High

NHTSAMay 18, 2023Nationwide• ALTEC

International MV (International) – Backup Light Issue (2023)

Navistar, Inc. (Navistar) is recalling certain 2000-2003 International 8100, 2001-2003 International 9100i, 2001-2007 International 9400i, 2001-2010 International 9200i, 2002-2007, 2009 International 8500, 2003-2007, 2013 International 9900i, 2003-2018 International 8600, 2004, 2007 International 9900iX, 2008-2018 International ProStar, 2010-2011, 2013, 2016 International LoneStar, 2011-2012, 2016 International 4400, 2017-2024 International LT, 2018-2024 International RH, 2019-2021 International LS, 2019-2024 International MV vehicles. The back-up lights offer low visibility when the vehicle is in reverse and bobtail mode. Also, the vehicles have not been equipped with additional unobstructed back-up lights. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment."

High

NHTSAMay 18, 2023Nationwide• INTERNATIONAL

Undeclared peanut

Class IIModerate

FDAMay 18, 2023CA, CO, FL +11 more• Werner Gourmet Meat Snacks, Inc.

Foretravel Realm (Foretravel) – Electrical System Failure (2023)

Foretravel, Inc. (Foretravel) is recalling certain 2022-2024 Realm, Realm Presidential, and FS450 motorhomes. The vehicle control module (ICM) may have a software error, which can cause a loss of drive power or disable other safety systems, such as the headlights or windshield wipers.

High

NHTSAMay 17, 2023Nationwide• FORETRAVEL

Access Hybritech p2PSA Reagent (Beckman) – Blocking Reagent Concentration (2023)

Reagent lot numbers include an insufficient concentration of blocking reagent.

Moderate

FDAMay 17, 2023CA, CO, CT +16 more• Beckman Coulter, Inc.

TYR Anamix Early Years Infant Formula (Nutricia) – undeclared tyrosine (2023)

Undeclared Allergen

Infant formula contains undeclared tyrosine

Class IIModerate

FDAMay 17, 2023AK, CA, CT +19 more• Nutricia North America

HeartWare VAD System (Heartware) – Monitor Logfile Issue (2023)

Medtronic has identified that the logfiles downloaded from the recently updated Model 1521 monitors (Serial Numbers: MON4xxxxxx for OUS and MON5xxxxxx for US), are unable to be processed by the Autologs web portal.

Low

FDAMay 16, 2023Nationwide• Heartware, Inc.

Western Star 57X (Western Star) – Turn Signal Malfunction (2023)

Fire/Burn Risk

Daimler Trucks North America, LLC (DTNA) is recalling certain 2023 Western Star 57X vehicles. The interior turn signals may flash too quickly and not align with the exterior turn signal flashing. Interior turn signals that consistently flash too quickly may not change their flash rate to alert the driver to replace the bulbs. An exterior turn signal bulb that is burnt out will not illuminate. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment."

High

NHTSAMay 16, 2023Nationwide• WESTERN STAR

Stay Informed

Maquet Medical Systems USA Recalls

Recall Summary

QUADROX-i Neonatal (Maquet) – Packaging Pinhole Risk (2023)

Medline Probe Cover Kits (Medline) – Barrier Seam Inadequacy (2023)

Aesculap Surgical Needle (Aesculap) – Product Code Mismatch (2023)

QUADROX-i Pediatric (Maquet) – Packaging Accessory Damage (2023)

PhysiciansCare Allergy Tablets (Acme United) – medication issue (2023)

Altec Aerial Device (Altec) – Strobe Water Leak (2023)

International MV (International) – Backup Light Issue (2023)

QUADROX-i Small (Maquet) – Packaging Accessory Damage (2023)

QUADROX-i Neonatal (Maquet) – Packaging Accessory Damage (2023)

Venous Hardshell Cardiotomy Reservoir (Maquet) – Packaging Pinhole Risk (2023)

QUADROX-i Small Adult (Maquet) – Packaging Pinhole Risk (2023)

QUADROX-iD Adult (Maquet) – Packaging Pinhole Risk (2023)

QUADROX-iD Adult (Maquet) – Packaging Accessory Damage (2023)

QUADROX-i Small Adult (Maquet) – Packaging Accessory Damage (2023)

Chili Cacahuate Japones (Werner) – undeclared peanut (2023)

Foretravel Realm (Foretravel) – Electrical System Failure (2023)

Access Hybritech p2PSA Reagent (Beckman) – Blocking Reagent Concentration (2023)

TYR Anamix Early Years Infant Formula (Nutricia) – undeclared tyrosine (2023)

HeartWare VAD System (Heartware) – Monitor Logfile Issue (2023)

Western Star 57X (Western Star) – Turn Signal Malfunction (2023)