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Last updated: February 2022
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Recall class: Type II
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Displaying 1 - 15 of 27 items.
Bd Alaris
Recall is being initiated to notify customers to the risk of the use and installation of unauthorized, third-party parts on the Alaris system.
Recall start date: Feb 7, 2022
RecallHealth product recall | 2022-02-28
Cardiohelp-I
Maquet Cardiopulmonary Gmbh has determined during the testing of a Cardiohelp-I, that the cylindrical pin in the upper part of the transport guard can come loose. the transport guard is an accessory of the Cardiohelp-I and secures the oxygenator to the…
RecallHealth product recall | 2022-02-28
Clearchoice Foam Face Shields
Southmedic had engaged an alternative material supplier due to material shortages and was made aware on January 25, 2022 that manufactured and distributed Clearchoice foam face shields have the potential for the presence of latex in the elastic bands of…
RecallHealth product recall | 2022-02-25
Rapid Protectant Hand Sanitizer Gel: labelling
Affected lot(s) may be missing risk statements and the non medicinal ingredient carbomer on the outer label.
RecallHealth product recall | 2022-02-23
Octagam 10% (Immune globulin intravenous, Human):Quality issue
Elevated reporting rate of hypersensitivity reactions in affected lot.
RecallHealth product recall | 2022-02-23
Vidas High Sensitive Troponin I (Tnhs)
Since January 2021, based on complaints received from the field related to critical non-repeatable overestimated results (changing interpretation according to the cutoff value, 19 ng/l, in the frame of the three hours algorithm that lead to a change in…
RecallHealth product recall | 2022-02-21
Sonialvision G4
As a result of Shimadzu investigation, it was determined that there is an issue with the adjustment procedure documented for the calibration of the system x-ray generator. This could cause x-ray radiation dose rate to exceed regulation and/or standards…
RecallHealth product recall | 2022-02-21
Quantum Blue Anti-Infliximab
Positive, instead of negative, results have been reported by customers for the low control and patient samples for Quantum Blue® Anti-Infliximab production Series 1107. The increased false-positive rate was confirmed internally at Bühlmann. Approximately…
RecallHealth product recall | 2022-02-14
Needle Free Dispensing Pins
Investigations conducted at the manufacturing site identified that the lot may present an elevated risk of leakage from the air-inlet filter of the device.
Recall start date: Jan 25, 2022
RecallHealth product recall | 2022-02-14
Needle Free Dispensing Pins
Investigations conducted at the manufacturing site identified that the lot may present an elevated risk of leakage from the air-inlet filter of the device.
Recall start date: Jan 25, 2022
RecallHealth product recall | 2022-02-14
Magec 1
Post-implantation fracture of an internal metallic component (i.e., locking pin) had been observed in early version of Magec rods that were manufactured prior to March 26, 2015. In June 2019, Nuvasive Specialized Orthopedics issued a safety alert to…
RecallHealth product recall | 2022-02-14
Carescape Central Station
If the Carescape Central Station v2.0 is used with an unapproved keyboard that contains a mute key, and if the mute key is pressed, the audio will be muted resulting in loss of audible alarms. this issue can result in a delay in noticing a change in…
RecallHealth product recall | 2022-02-14
Welch Allyn Diagnostic Cardiology Products
Hillrom has become aware of a vulnerability which allows the entry of any username that is provisioned in the application without supplying a password. This will then grant access to the application with the privileges of the username provided. the…
RecallHealth product recall | 2022-02-14
Heartware Ventricular Assist System
While performing a review of product literature, including the instructions for use (IFU) and patient manual (PM), It was identified that additional clarity was required around cleaning the power source connectors (controller AC adapter, DC adapter, and…
RecallHealth product recall | 2022-02-14
Ysio Radiography X-Ray System - Full Motorized
Siemens is issuing a preventive update of the system software to exclude any potential hazard of unexpected system movement.
Recall start date: Feb 7, 2022
RecallHealth product recall | 2022-02-14