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Out of specification result for assay test in the affected lots

As a result of a supplier notification, Philips determined that certain devices were built with motor assemblies that could contain non-conforming plastic material. If the non-conforming plastic is present in the device motor, it could lead to off-…

Stryker has identified a nonconformance within two specific lots of evolve proline stems. Specifically, the outer label does not match the device inside the package. the affected lot of evolve proline stem 7.5mm +2 contains a size 9.5mm +4 stem, while…

Expired products were shipped to customers. Recall start date: August 17, 2022

Medtronic is issuing a voluntary medical device correction related to specific serial numbers of the turbine component of Puritan Bennett 500 series ventilators. This voluntary medical device correction is being issued following confirmation of six…

Affected lot may contain particulate matter  

Jamp Pharma Corporation is recalling one lot (D10776B) of Jamp-Atorvastatin Calcium after one bottle labelled to contain 10 mg tablets of Jamp-Atorvastatin Calcium was found to contain 40 mg tablets of Jamp-Atorvastatin Calcium. Pharmacists may not…

Affected lot may contain the presence of particles

Ecotest Covid-19 Antigen Rapid Test Devices were sold without having the proper authorization from Health Canada. Recall start date: August 11, 2022

Cardinal Health was recently informed of a field action recall from icu medical concerning the microclave clear connector referenced above. The recall is being issued due to the potential for a manufacturing defect within specific lots of microclave…

Pharmascience Inc. is recalling one lot of pms-Hydromorphone, 2 mg tablets, (lot 639268) as the bottles may contain hydromorphone tablets of a different strength (8 mg), meaning they contain higher amounts of hydromorphone. Products from the affected lot…

The dissolution for vitamin D3 is out of specification in the affected lots.

Merit Medical Systems, Inc. is voluntarily conducting a recall of the Corvocet™ Biopsy System due to a product defect resulting from incorrect assembly. Merit was made aware of the defect as a result of five (5) customer complaints (no adverse/reportable…

On the Ortho Optix Reader, when reviewing the results, the user can edit a grade and/or analysis of the results. • When performing this action, the user may also choose to "cancel" the edit. •Wwhen cancelling the edit, the user is informed that the "…

Olympus conducted an investigation after receiving seven complaints globally regarding parts moving freely on the shaft of the device. Through the investigation, Olympus identified that certain lot numbers of Powerseal may have an out of specification…