Search

Results of post market surveillance revealed that under certain circumstances the room configuration parameters of the system are set to default values. If these values are larger than the actual room dimensions, a collision with the ceiling or wall…

Siemens Healthcare is informing customers with a preventive measure to exclude any potential risk of patient injury caused the footrest detaching from the patient table during an examination. Recall start date: December 15, 2022

Siemens Healthcare Diagnostics Inc. has confirmed an issue through complaint investigation. The issue has the potential to affect the recovery of po2 in quality control (qc) at elevation with barometric pressures <730 mmhg on epoc sensor configuration…

Gas cylinders containing commercial grade oxygen instead of medical grade oxygen were delivered to homecare customers.

Emergent received 3 complaints from customers between 18 Oct 2022 - 15 Nov 2022 related to leaking packets. Product in leaking packets may not perform as effectively as intended.  Recall start date: November 24, 2022

Some electrode pads used with the hs1/onsite/home AED have been observed to experience gel separation from the foam/tin backing when peeled from the yellow plastic liner. The gel may fold onto itself, resulting in reduced surface area of gel on the pad.…

The concentration of the medicinal ingredient, sodium fluoride, is out of specification in the affected lot.

The software may not be able to identify that the orders are for the same patient and may not perform the discrepant result checks. Recall start date: November 18, 2022

There is a potential for false positive results for flu B and RSV while using the list numbers and lot numbers referenced above associated with the manufacture of these lots. There is also a potential for delayed results when using these lots as reactive…

This recall addresses a product concern regarding the drapes in the kit. The supplier (3M) decided to recall the drapes in the kit because it was confirmed that the liner on the adhesive component of the affected drapes is difficult to remove without…

Affected lot may result in a false negative for skin test (peanut allergy).

Product sterility may be compromised in the affected lot.

Affected lot contains active ingredient (Cholecalciferol) levels outside of the labelled claim.

The colour is out of specification in the affected lot(s).

Affected lots may contain the presence of foreign matter.