Search
Returning search results with filters:
Remove filter for
Audience: Hospitals
Remove filter for
Recall class: Type I
Clear all
Type
Audience
Category
Issue
Last updated
Recall class
Please note: using the search filters may not provide accurate search results for records prior to November 2021. When searching for older records, please ensure that you use the include archived checkbox.
Displaying 1 - 15 of 30 items.
DRAXIMAGE MDP: Affected lot may contain particulate matter
Affected lot may contain particulate matter
RecallHealth product recall | 2022-08-30
NERFASIN 20: Affected lot may contain the presence of particles
Affected lot may contain the presence of particles
RecallHealth product recall | 2022-08-29
PMS-Hydromorphone: Affected lot may contain tablets that could potentially lead to overdose
Pharmascience Inc. is recalling one lot of pms-Hydromorphone, 2 mg tablets, (lot 639268) as the bottles may contain hydromorphone tablets of a different strength (8 mg), meaning they contain higher amounts of hydromorphone. Products from the affected lot…
RecallHealth product recall | 2022-08-22
Sodium Chloride Inj; Glass particles
The affected lots may contain glass particles.
RecallHealth product recall | 2022-08-02
Nim™ Standard Reinforced Emg Endotracheal Tube & Nim Contact™ Reinforced Emg Endotracheal Tube
Manufacturer has received reports of events related to airway obstruction while using the impacted device. Not following the instructions for use (IFU) and over-inflating the cuff increases intra-cuff pressure, which can cause the silicone cuff to extend…
RecallHealth product recall | 2022-05-10
Breathing System Filter Safestar 55
Dräger has become aware of one case in which an obstructed Breathing System Filter Safestar 55 was used on a patient during anesthesia. The patient reportedly became hypoxic and had to be reanimated. If an obstructed filter is used on a patient,…
RecallHealth product recall | 2022-05-10
Dragonfly Opstar Imaging Catheter
The proximal marker on devices from these lots may separate from the device. A dislodged marker may require additional intervention, including unplanned additional coronary intervention, or surgery. To date Abbott has received 5 complaints related to…
RecallHealth product recall | 2022-04-25
Cortrak*2 Enteral Access System (Eas)
Avanos medical is conducting a voluntary field correction for the Cortrak* 2 Enteral Access System (Eas) because modifications to the labeling of the device have been initiated. Reports of injuries and patient deaths related to misplacement of…
RecallHealth product recall | 2022-04-19
Fabian HFOi Ventilator
Bias flow selection for NO system usage is missing from the user interface of Fabian HFOi Ventilators following incorrect selection of device configuration during a software update. This is caused by human error and there is no defect in the device or…
RecallHealth product recall | 2022-04-12
Medfusion Syringe Infusion Pumps
Smiths Medical became aware of eight (8) issues-(identified below) that can potentially occur that may impact therapy delivery in specific Medfusion 3500 and 4000 syringe infusion pumps.
1. Primary Audible Alarm (PAA)
2. Unanticipated depleted battery…
RecallHealth product recall | 2022-04-11
Optima Mr430s 1.5t - Main Unit
Potential for injury if the MR system is incorrectly deinstalled.
Recall start date: Mar 10, 2022
RecallHealth product recall | 2022-03-21
Optima Mr450w
Potential for injury if the MR system is incorrectly deinstalled.
Recall start date: Mar 10, 2022
RecallHealth product recall | 2022-03-21
Optima Mr360
Potential for injury if the Mr system is incorrectly deinstalled.
Recall start date: Mar 10, 2022
RecallHealth product recall | 2022-03-21
Med-Rx Medication/Primary Solution Administration Kit
BBMI has identified through complaints the potential for fluid leakage or low fill volume of the respective containers of 0.9% sodium chloride injection USP 250ml [din : 01924303, lot no : l8002]. There is also the potential for smaller micro-leaks which…
RecallHealth product recall | 2022-03-14
Infinity Centralstation Wide
The recall is being initiated due to a software defect that is triggered by disconnecting / connecting an USB device, causing a restart of the infinity central station and a temporary loss of central monitoring.
Recall start date: Mar 8, 2022
RecallHealth product recall | 2022-03-14