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Displaying 1 - 15 of 295 items.
Affected lots are missing risk statements on the bottle.
RecallHealth product recall | 2023-09-26
Olympus found that certain lots of the CV-190 do not start up properly and as a result, the image from the endoscope is not displayed when the operations listed below are performed because parts that deviated from the specification were assembled into…
RecallHealth product recall | 2023-09-22
Affected lot may contain the presence of glass particulate.
RecallHealth product recall | 2023-09-20
Affected lot may be OOS for related compound CZ RC1
RecallHealth product recall | 2023-09-19
The shaft and tip component of the Universal Joint Screwdriver was manufactured with the incorrect raw stainless steel material.
Recall start date: September 1, 2023
RecallHealth product recall | 2023-09-18
Affected lot may not be filled with the correct amount of leuprolide acetate.
RecallHealth product recall | 2023-09-12
Siemens Healthcare will be informing customers about potential dot- or line-shaped artifacts caused by the presence of lubricating grease within the headband of the over-ear headphones listed below when used during head examinations with the Magnetom MRI…
RecallHealth product recall | 2023-09-11
Immucor, Inc. has indicated that this medical device recall is to communicate that some vials of Capture-CMV indicator red cells may contain particulates. The particulates are associated with fungal growth in the vials.
Recall Start Date: August 24,…
RecallHealth product recall | 2023-09-11
Affected lots contain magnesium levels outside of the labelled claim.
RecallHealth product recall | 2023-09-08
Arjo has observed an increasing complaint trend on the following failure modes occurring on Arjo medical beds assembled with the Indigo modules: unanticipated device self-acceleration while being operated by a caregiver, unexpected movement without any…
RecallHealth product recall | 2023-09-08
Some Phoroptor VRx devices may have an assembly defect that causes the device to detach from the bracket that connects it to an ophthalmic stand. A device that detaches from a stand can fall on to a patient or operator causing an injury. The defect was…
RecallHealth product recall | 2023-09-08
The Equipro High Frequency Portable EI-113P is non-compliant (not licensed for sale in Canada) as a Class II medical device under Canadian law. Further distribution or use of the remaining product must stop immediately. Please notify any customers to…
RecallHealth product recall | 2023-09-08
Affected lot may result in a false negative for skin test (pecan nut allergy)
RecallHealth product recall | 2023-09-07
The total combined yeasts and molds count is out of specification for the affected lot.
RecallHealth product recall | 2023-09-07
The stability assay is out of specification in the affected lots.
RecallHealth product recall | 2023-09-06