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Last updated: February 2022
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Last updated: 2022
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Displaying 1 - 15 of 37 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
0.9% Sodium Chloride Injection USP: Leaking solution bag
Solution bags may be leaking in affected lot.
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 antigen test kits and potential exposure to hazardous substances
Following an increase in reports to poison control centres, Health Canada is advising Canadians about potential risks associated with the misuse or accidental ingestion or spillage of COVID-19 rapid antigen test kit solutions on the skin. Health Canada…
AlertPublic advisory | 2022-02-24
Distribution of NUVAXOVID with English-only Vial and Carton Labels
NUVAXOVID was authorized by Health Canada on February 17, 2022. In order to provide earlier access to NUVAXOVID in the context of the global pandemic, Novavax, Inc. will distribute product vials, cartons and package inserts that are in English only for a…
AlertHealth professional risk communication | 2022-02-23
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
Odan Itraconazole: Out of specification
The assay is out of specification in the 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
Temperature Probes
The esophageal/rectal/skin temperature probe's instructions for use, (IFU), contain inadequate instructions related to the cleaning and disinfection process for the reusable probes. The IFU instructs the user to clean the product with disinfecting agents…
RecallHealth product recall | 2022-02-21
Baxter Corporation’s MiniCap Extended Life Peritoneal Dialysis Transfer Sets: Certain cleaning products, including hand sanitizers and solvents, may damage sets
Health Canada is advising patients who use MiniCap Extended Life Peritoneal Dialysis Transfer Sets, manufactured by Baxter Corporation, that direct contact between the sets and certain cleaning products, including hand sanitizers and solvents, may damage…
AlertPublic advisory | 2022-02-16
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