FDA Alerts: Medtronic Model 8637 SynchroMed II Implantable Infusion Pump
Monday 12 September 2011 at 2:20 pm September 12, 2011: The FDA reports that, for the Medtronic Model 8637 SynchroMed II Implantable Infusion Pump, there is a Class I Recall due to the potential for reduced battery performance that can lead to the sudden loss of therapy and the return of underlying symptoms and/or therapy withdrawal symptoms.FDA Alerts: Risperdal and Risperidone
Tuesday 21 June 2011 at 12:00 pm
Risperidone (Risperdal) and Ropinirole (Requip): Medication
Errors - Name Confusion
Healthcare Professionals reminded to clearly print or spell out the
medication name on prescriptions.
Risperdal (risperidone) and Risperidone: Recall -
Uncharacteristic Odor
Two lots recalled. Contamination thought to be the result of a
chemical preservative applied to wood used in the construction of
pallets on which materials are transported and stored.
