All Recalls

92,900 total recalls in our database

Azurion 5 M12 System Code: (1) 722227 (2) 722231

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

๐Ÿฅ Medical Devices Class I - Dangerous

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

Jan 13, 2025 Other Medical Devices Nationwide View Details โ†’
๐Ÿฅ Medical Devices Class I - Dangerous

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

Jan 13, 2025 Other Medical Devices Nationwide View Details โ†’

Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

๐Ÿฅ Medical Devices Class I - Dangerous

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

Jan 13, 2025 Other Medical Devices Nationwide View Details โ†’
๐Ÿฅ Medical Devices Class I - Dangerous

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

Jan 13, 2025 Other Medical Devices Nationwide View Details โ†’

Disposable set may leak during priming from a female quick connector due to a crack in the female quick connector, may lead to a potential delay in treatment since the set will need to be replaced by another set

Jan 2, 2025 Infusion Pumps Nationwide View Details โ†’

Allura Xper FD20/20 System Code: (1) 722038

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

๐Ÿฅ Medical Devices Class I - Dangerous

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

Jan 13, 2025 Other Medical Devices Nationwide View Details โ†’
๐Ÿฅ Medical Devices Class I - Dangerous

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

Jan 13, 2025 Other Medical Devices Nationwide View Details โ†’

Due to manufacturing issue (unintended by-product of the injection molding process) a sharp pin that may puncture the blister packaging and breaching the sterile barrier of the finished product.

Jan 10, 2025 Implants & Prosthetics Nationwide View Details โ†’

Due to nasal spray stability failure for bioburden.

Dec 28, 2024 Other Medical Devices Nationwide View Details โ†’
๐Ÿฅ Medical Devices Class I - Dangerous

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

Jan 13, 2025 Other Medical Devices Nationwide View Details โ†’
๐Ÿฅ Medical Devices Class I - Dangerous

The user can continue to take the next exposure after reaching the Automatic Exposure Control (AEC) limit, without taking any further actions to acknowledge or adjust exposure techniques. In all cases, a message still appears on the screen when the AEC limit is reached.

Jan 28, 2025 Diagnostic Equipment Nationwide View Details โ†’
๐Ÿฅ Medical Devices Class I - Dangerous

Certain definitive dental implant restoration cases may have included a temporary titanium abutment (cylinder), rather than a definitive titanium abutment, which may lead the titanium abutment fracture, which may risk loosening of the affixed restoration; fragments could also injure oral mucosa, and could be aspirated.

Dec 6, 2024 Other Medical Devices Nationwide View Details โ†’
๐Ÿฅ Medical Devices Class I - Dangerous

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

Jan 13, 2025 Other Medical Devices Nationwide View Details โ†’

Sutures may have an open seal on the primary packaging, due to a manufacturing issue on a specific machine, and if issue is undetected could lead to breach in sterility, could introduce pathogens to the patient and cause infection.

Dec 20, 2024 Surgical Instruments Nationwide View Details โ†’

Allura Xper FD10C System Code: (1) 722001

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

๐Ÿฅ Medical Devices Class I - Dangerous

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

Jan 13, 2025 Other Medical Devices Nationwide View Details โ†’

Sysmex was made aware of a report of false results due to carry-over caused by the sporadic omission of the probe wash step during antibody pipetting on the PS-10 Sample Preparation System.

Jan 6, 2025 Other Medical Devices Nationwide View Details โ†’
๐Ÿ  Consumer Products Class III - Low Risk

The recalled snow thrower impeller and auger assembly can continue rotating even after the operator control lever is released, posing a laceration hazard if a user makes contact with the rotating parts inside the housing enclosure at the front of the machine.

Feb 6, 2025 Other Consumer Products Nationwide View Details โ†’