All Recalls

95,018 total recalls in our database

Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.

Feb 6, 2024 Other Foods View Details →

Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case

Jan 30, 2024 Other Medical Devices Nationwide View Details →

Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case

Jan 30, 2024 Other Medical Devices Nationwide View Details →

Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case

Jan 30, 2024 Other Medical Devices Nationwide View Details →

Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"

Mckesson Medical-Surgical Inc. Corporate Office

🏥 Medical Devices Class I - Dangerous

Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In refrigerator due to mechanical failures, causing temperatures to fall below the validated range of 35.6 - 46.4 Degrees Fahrenheit (2 - 8 Degrees Celsius) for up to 60 minutes which could increase the probability of an incorrect test result or a delayed test result.

Jan 9, 2024 Diagnostic Equipment Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

Natus has become aware that its third-party supplier Parker Laboratories Inc. is conducting a voluntary recall related to their Tensive Conductive Adhesive Gel, Ref. 22-60 Lot Number A0623009. They have received five complaints. These customers reported that the gel is too thick, is discolored (darker than usual), and in one instance, patients reported irritation after procedures using the gel.

Feb 7, 2024 Infusion Pumps Nationwide View Details →

Observed outflow graft deformation known as Extrinsic Outflow Graft Obstruction (EOGO) associated with Left Ventricular Assist System.

Feb 19, 2024 Implants & Prosthetics Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

When a paraPAC plus ventilator is switched to the operating mode of VENTILATE, the ventilator may intermittently provide continuous positive gas flow instead of the intended cycling like a human breath. This non-cycling and continuous positive gas flow when in the cycling mode, is a malfunction, not allowing the ventilator to properly function as designed.

Feb 7, 2024 Patient Monitors Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case

Jan 30, 2024 Other Medical Devices Nationwide View Details →