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Displaying 1 - 15 of 5414 items.
This recall involves one lot of Vortex Cannabis Inc.’s 10 SOUR THC JELLY DROPS 10 MG THC PER DROP edible cannabis one lot of Vortex Cannabis Inc.’s 10 MIXED BERRY JELLY DROPS 10MG THC edible cannabis sold through authorized retailers in Ontario.…
RecallConsumer product recall | 2022-08-05
The recalled products do not meet the labelling requirements and the child-resistant packaging requirements of the Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act.
The lack of child-resistant…
RecallConsumer product recall | 2022-08-05
The recalled pet food may be contaminated with Listeria monocytogenes, posing a risk of cross contamination and illness after handling the pet food.
Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in…
RecallConsumer product recall | 2022-08-05
Mother Dairy brand Paneer Fresh Cheese recalled due to generic E. coli.
The recalled product was sold in Alberta.
RecallNotification | 2022-08-04
One client reported that HL7 files transferred to an outbound results interface (specific to one client) would sometimes contain more than one patient identifier, which could lead to results being assigned to the wrong patient in a third party system…
RecallHealth product recall | 2022-08-04
Solution bags may be leaking in affected lot.
RecallHealth product recall | 2022-08-04
The rear guard assembly can break or detach, posing a laceration hazard to the user.
As of June 13, 2022, the company has received one report of a laceration injury in Canada. In the United States, the company has received reports of 8 laceration…
RecallConsumer product recall | 2022-08-04
The affected lots may contain glass particles.
RecallHealth product recall | 2022-08-02
Baxter Corporation is issuing an urgent medical device recall for all non-expired lots of Self-Righting Luer Slip And Luer Lock Tip Caps listed due to the potential of the packaging seal not maintaining a sterile barrier for the tip caps.
Recall start…
RecallHealth product recall | 2022-08-02
For some insulin mentor feature users, there is an overlap in their time-intervals. this causes the system to provide an incorrect insulin recommendation to the user and could potentially result in a deviation from the value the user should be getting…
RecallHealth product recall | 2022-08-02
A software defect is present where in the case that the customer is running on smart last cycle, and a procedure is aborted or has an unrecoverable interruption, the red blood cell loss estimation flag may not be accurate, and should not be used as the…
RecallHealth product recall | 2022-08-02
Distance and area measurements can display inaccurate measurement values that are overestimated (measurement size is larger than true size) when a study is launched in global stack viewport on centricity universal viewer and universal viewer. …
RecallHealth product recall | 2022-08-02
The field action FMI 32067/ and customer communication, plus enhanced panel design were launched in March 2019 and July 2020, respectively. However, GE Healthcare recently received one complaint of a patient fall related to the bedside panels not being…
RecallHealth product recall | 2022-08-02
Some cartons of the lot of Vitek 2 Ast cards have been identified as impacted by a card and/or card label mix issue during production at the manufacturing site. The card and label of the card are incorrect and are from another Vitek 2 ID or AST…
RecallHealth product recall | 2022-08-02
Ortho Clinical Diagnostics (Ortho) became aware of an anomaly that affects Vitros Xt 3400 and Vitros Xt 7600 systems. These systems utilize a digital imaging reflectometer and led light source to generate Vitros microslide assay results. Ortho's on-going…
RecallHealth product recall | 2022-08-02