All Recalls

95,064 total recalls in our database

Presence of Particulate Matter: Product complaints received of grey flecks, identified as shredded rubber particulate matter from the stopper observed in reconstituted vials.

Dec 20, 2018 Prescription Drugs Nationwide View Details →

Presence of Particulate Matter: Foreign matter identified as glass detected in Vecuronium Bromide for Injection.

Jan 3, 2019 Prescription Drugs Nationwide View Details →

Presence of Particulate Matter: Product complaints received of grey flecks, identified as shredded rubber particulate matter from the stopper observed in reconstituted vials.

Dec 20, 2018 Prescription Drugs Nationwide View Details →

Presence of Particulate Matter: Product complaints received of grey flecks, identified as shredded rubber particulate matter from the stopper observed in reconstituted vials.

Dec 20, 2018 Prescription Drugs Nationwide View Details →

Presence of Particulate Matter: Product complaints received of grey flecks, identified as shredded rubber particulate matter from the stopper observed in reconstituted vials.

Dec 20, 2018 Prescription Drugs Nationwide View Details →

Presence of Particulate Matter: Foreign matter identified as glass detected in Vecuronium Bromide for Injection.

Jan 3, 2019 Prescription Drugs Nationwide View Details →

After an upgrade of the software of the Overhead Tube Crane, there were isolated cases in which the Overhead Tube Crane movement does not stop when the movement button is released. Instead of stopping while the movement button is released, the Tube Head Crane moves to the intended position.

Dec 4, 2018 Diagnostic Equipment Nationwide View Details →

Supplier had changed its resin sub-suppliers three (3) times without notifying BSC. These changes resulted in slight variations in resin material compositions which were not reflected in BSC s internal product documentation. Not approved in customer document.

Nov 28, 2018 Diagnostic Equipment View Details →

A component of the device was recalled by a supplier. In rare cases of inadequate maintenance or very high clinical workload, the first steel wire rope of the lifting column, which is designed to take the load, can break without triggering the safety lock. This can lead to overloading of the safety cable, which is not designed to permanently carry the load of the lifting column or continuously move under load. This could cause material fatigue and cause the arm to drop unexpectedly during patient positioning. If the arm drops unexpectedly, patients and users may be seriously injured.

Nov 14, 2018 Diagnostic Equipment View Details →

Ingenia Elition S, Ingenia Elition X

Philips Medical Systems Nederlands

🏥 Medical Devices Class I - Dangerous

During automatic tabletop movement, pressing and holding the Stop Table button may lead to an unexpected restart of the table movement.

Dec 3, 2018 Other Medical Devices View Details →