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Displaying 1 - 15 of 272 items.
The dissolution for vitamin D3 is out of specification in the affected lot.
RecallHealth product recall | 2022-06-22
Siemens Healthcare Diagnostics Inc. has confirmed the occurrence of inconsistent discrepant (low bias) po2 results. at a medical decision level of approximately 80mmhg, the maximum negative bias is - 11.7% (the acceptable bias is +/-10% for po2 range 50-…
RecallHealth product recall | 2022-06-20
Rocky Mountain Soap Company recalls all lots of two Broadspectrum solar protection products due to quality concerns linked to deficiencies in Good Manufacturing Practices (GMP). The microbial content/ total aerobic microbial content may be out of…
RecallHealth product recall | 2022-06-16
Quality concerns of affected lots due to deficiencies in Good Manufacturing Practices (GMP). May contain undeclared impurity, methanol, at elevated levels.
RecallHealth product recall | 2022-06-16
Notification to inform customers of a potential issue relating to pump's battery cap and provide actions required by the customers. Notification advises customers that if the metal contact becomes loose or falls off from the…
RecallHealth product recall | 2022-06-13
During the manufacturing process, there is a slight risk of the formation of a hole in the sterile packaging which typically forms near the pre-sealed area at the bottom of the sterile packaging of the Yelloport Elite Universal Seals.
Recall start…
RecallHealth product recall | 2022-06-13
Unauthorized KN95/FFP2 particulate respirator mask - do not use as a respirator.
Recall start date: May 10, 2022
RecallHealth product recall | 2022-06-07
Software update required. a change was made to v3.00 (released june 30, 2021) to update bit11 in HST file flag. This was done for compatibility with clearlink website- discovered 0inch/9inch inconsistency when testing for Arcutis clinical trial data…
RecallHealth product recall | 2022-06-07
Presence of an unspecified impurity near the acceptable concentration limit in the affected lot.
RecallHealth product recall | 2022-06-02
Surestrips Rapid Response Covid-19 Antigen Rapid Test Device are not authorized for sale in Canada as they were re-packaged into single tests and re-labelled without authorization by the manufacturers listed on the label (i.e.…
RecallHealth product recall | 2022-05-30
Surestrips Covid-19 Antigen Tests are not authorized for sale in Canada as they were re-packaged into single tests and re-labelled without authorization by the manufacturers listed on the label (i.e. Artron Laboratories Inc.).
Recall start date…
RecallHealth product recall | 2022-05-30
The encrypted barcode data generates an error that prevents the analyzer from using the entire contents of the bottle. The user is required to replace the reagent container prematurely. On 4/25/22, the issue was identified through the trending of post…
RecallHealth product recall | 2022-05-30
An end user site attempted to perform QC on a single test using multiple QC kits. The QC module was not designed to support testing of multiple QC kits for a single test, and it is required that all QC samples used to validate a test are contained in a…
RecallHealth product recall | 2022-05-30
Mold was found in lot Y591676 of the product. Two species of mold were identified that could pose a potential health risk to users.
Recall start date: May 3, 2022
RecallHealth product recall | 2022-05-30
Label does not meet Health Canada requirements
RecallHealth product recall | 2022-05-27