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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

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…

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…

Cook Medical identified that devices from the affected device lots may have a breach of the chevron seal of the packaging. therefore, the sterility of affected devices may be compromised. Recall start date: August 16, 2022

Manufacturer internally detected a potential operational software issue affecting Cobas Pure E 402, Cobas Pro and/or Cobas 8000 E 801 instruments. The issue may occur under specific instrument conditions and sequence of laboratory actions when the quick…

Contains undeclared impurity, benzene, at elevated levels.

Recall due to a potential fit issue with some Clarity™ aligners and Clarity™ retainers. Recall start date: July 13, 2022

Connection issue for Vanta pain pc implantable neurostimulators when transplanted in the same patient. "Too many devices" error will appear from Clinician Programmer Application (CPA) when there is more than 1 Vanta ins detected by the clinician…

Notification to inform customers that in rare instances (0.085%) during initial programming, the Vanta CP app will display the error code 1502 message because the Vanta INS reset block id log is full. Once the log is full, all subsequent interrogations…