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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

581

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 1921–1940 of 10937 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

Fexofenadine Tablets (Perrigo) – Impurities Spec Failure (2023)

Failed Impurities/Degradation Specifications

Class IIModerate

FDAFeb 9, 2023Nationwide• L. Perrigo Company

Fexofenadine Tablets 180mg (Perrigo) – Impurities Spec Failure (2023)

Failed Impurities/Degradation Specifications

Class II

1...95 969798 99...547

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Moderate

FDAFeb 9, 2023Nationwide• L. Perrigo Company

Allergy Relief Tablets (Perrigo) – Impurities Spec Failure (2023)

Failed Impurities/Degradation Specifications

Class IIModerate

FDAFeb 9, 2023Nationwide• L. Perrigo Company

Fexofenadine Tablets (Perrigo) – Impurities Spec Failure (2023)

Failed Impurities/Degradation Specifications

Class IIModerate

FDAFeb 9, 2023Nationwide• L. Perrigo Company

Picnic Allergy Tablets (Perrigo) – Impurities Spec Failure (2023)

Failed Impurities/Degradation Specifications

Class IIModerate

FDAFeb 9, 2023Nationwide• L. Perrigo Company

Allergy Relief Tablets (Perrigo) – Impurities Spec Failure (2023)

Failed Impurities/Degradation Specifications

Class IIModerate

FDAFeb 9, 2023Nationwide• L. Perrigo Company

Non-Drowsy Allergy Relief (Perrigo) - Impurity Specifications (2023)

Failed Impurities/Degradation Specifications

Class IIModerate

FDAFeb 9, 2023Nationwide• L. Perrigo Company

ALLER-FEX Allergy Tablets (Perrigo) - Impurity Specifications (2023)

Failed Impurities/Degradation Specifications

Class IIModerate

FDAFeb 9, 2023Nationwide• L. Perrigo Company

Allergy Relief Tablets (Perrigo) – Impurities Spec Failure (2023)

Failed Impurities/Degradation Specifications

Class IIModerate

FDAFeb 9, 2023Nationwide• L. Perrigo Company

Fexofenadine Hydrochloride Tablets (Perrigo) - Impurity Specifications (2023)

Failed Impurities/Degradation Specifications

Class IIModerate

FDAFeb 9, 2023Nationwide• L. Perrigo Company

Allergy Relief Tablets (Perrigo) – Impurities Spec Failure (2023)

Failed Impurities/Degradation Specifications

Class IIModerate

FDAFeb 9, 2023Nationwide• L. Perrigo Company

Aller-Ease Allergy Tablets (Perrigo) - Impurity Specifications (2023)

Failed Impurities/Degradation Specifications

Class IIModerate

FDAFeb 9, 2023Nationwide• L. Perrigo Company

Allergy Relief Tablets (Perrigo) – Impurities Spec Failure (2023)

Failed Impurities/Degradation Specifications

Class IIModerate

FDAFeb 9, 2023Nationwide• L. Perrigo Company

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

Medtronic Grafton Gel (Medtronic) – Packaging Concern (2023)

Potential for packaging non-conformances directly related to the dual-barrier, sterile pouch packaging system. Non-conforming packaging may lead to a breach in the sterile barrier.

Low

FDAFeb 8, 2023Nationwide• Medtronic Sofamor Danek USA Inc

Medtronic Grafton Orthoblend (Medtronic) – Packaging Concern (2023)

Potential for packaging non-conformances directly related to the dual-barrier, sterile pouch packaging system. Non-conforming packaging may lead to a breach in the sterile barrier.

Low

FDAFeb 8, 2023Nationwide• Medtronic Sofamor Danek USA Inc

Medtronic Grafton DBF Inject (Medtronic) – Packaging Concern (2023)

Potential for packaging non-conformances directly related to the dual-barrier, sterile pouch packaging system. Non-conforming packaging may lead to a breach in the sterile barrier.

Low

FDAFeb 8, 2023Nationwide• Medtronic Sofamor Danek USA Inc

Medtronic Grafton Crunch (Medtronic) – Packaging Concern (2023)

Potential for packaging non-conformances directly related to the dual-barrier, sterile pouch packaging system. Non-conforming packaging may lead to a breach in the sterile barrier.

Low

FDAFeb 8, 2023Nationwide• Medtronic Sofamor Danek USA Inc

Medtronic Accelerate Grafton DBF (Medtronic) – Packaging Concern (2023)

Potential for packaging non-conformances directly related to the dual-barrier, sterile pouch packaging system. Non-conforming packaging may lead to a breach in the sterile barrier.

Low

FDAFeb 8, 2023Nationwide• Medtronic Sofamor Danek USA Inc