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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)

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 4521–4540 of 21320 recalls

BEQ-HLS Medical Set (Maquet) – Packaging Sterility Concern (2023)

Firm has initiated a removal of the product due to insufficient evidence of packaging sterility. Exposure to a non-sterile medical device may result in inflammation, infection, sepsis, or ischemia.

Low

FDAFeb 13, 2023Nationwide• Maquet Medical Systems USA

Global Total LP Medium (CooperSurgical) – Incorrect Medium (2023)

It has come to CooperSurgical's attention that the affected Product may contain a medium other than the Global Total LP single step medium which does not contain the protein source required for embryo culture and development.

Moderate

FDAFeb 13, 2023Nationwide• CooperSurgical, Inc.

IC Bus RESB (IC Bus) – Roof Panel Concern (2023)

Navistar, Inc. (Navistar) is recalling certain 2022-2024 IC Bus CE, 2022-2023 IC CE SBus, IC RE, and 2023 EV school buses. The roof panel may have been manufactured with insufficient joint strength. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 221, "School Bus Body Joint Strength."

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Moderate

NHTSAFeb 10, 2023Nationwide• IC BUS

IC Bus CE (IC Bus) – Roof Panel Concern (2023)

Navistar, Inc. (Navistar) is recalling certain 2022-2023 IC Bus CE, and 2022-2023 IC RE transit buses. The roof panel may have been manufactured with insufficient joint strength.

Moderate

NHTSAFeb 10, 2023Nationwide• IC BUS

da Vinci Surgical System (Intuitive) – Manipulator Component Issue (2023)

Due to Universal Surgical Manipulator (USM) instrument carriage being loose as a result of the linear rail component not being manufactured within specifications.

Moderate

FDAFeb 10, 2023Nationwide• Intuitive Surgical, Inc.

DreamStation CPAP (Philips) – Communication Problem (2023)

A limited number of remediated Philips DreamStation units may experience communication issues when connecting to the cloud-based care management application. Should this be the case, this may affect the ability to download prescription settings to the device or the device may have incorrect prescription settings for the patient.

Moderate

FDAFeb 10, 2023Nationwide• Philips Respironics, Inc.

Sodium Chloride Injection 1000ml (B. Braun) – Sterility Concern (2023)

Lack of sterility assurance: Recall of certain batches of 0.9% Sodium Chloride for Injection USP in EXCEL¿ Plus IV Container product due to the possibility of an incomplete seal that may cause leakage. The impacted lots may exhibit microscopic channel leaks near the port assembly of the product.

Class IIModerate

FDAFeb 10, 2023Nationwide• B. Braun Medical Inc.

Sodium Chloride Injection 500ml (B. Braun) – Sterility Concern (2023)

Class IIModerate

FDAFeb 10, 2023Nationwide• B. Braun Medical Inc.

E-Z-GO Personal Transportation Vehicles (Textron) – fire hazard (2023)

Fire/Burn Risk

This recall involves model year 2021, 2022 and 2023 Freedom and Valor E-Z-GO RXV personal transportation vehicles, with serial numbers ranging from 5585710 through 5716926; and model year 2021, 2022 and 2023 Valor, Express and Liberty E-Z-GO TXT personal transportation vehicles, with serial numbers ranging from 3478457 through 3591890. Recalled units are equipped with an optional USB charge port. The vehicle's serial number is printed near the base of the steering column for RXV models and is printed below the operator seat position for TXT models. These vehicles are commonly referred to as golf carts or golf cars and are used primarily to transport people.

High

CPSCFeb 9, 2023Nationwide• Textron Specialized Vehicles, of Augusta, Georgia

myQ Garage Door Control Panels (Chamberlain) – entrapment risk (2023)

This recall involves LiftMaster myQ garage door control panels, sold individually or with wall-mount residential jackshaft garage door openers. LiftMaster and myQ are printed on the front of the black control panels. The recalled control panels were manufactured between March 2022 and October 2022. The manufacture date, in MM/YY format, the model number and the UPC code are printed on a label located on the back of the unit. The following are the model numbers and UPC codes included in this recall: Model Numbers UPC Codes 8500MC 012381203536 8500CMC 012381203529 8500RGDMC 012381203543 RJO20MC 012381188246 RJO20CMC 012381191277 RJO20CHMC 012381191277 889LMMC 012381203611 889RGDMC 012381203628 041A7928-3MC 012381204304

Moderate

CPSCFeb 9, 2023Nationwide• Grupo Chamberlain S.de R.L. de C.V., of Mexico