Symptomtext
HCP called to report that an expired dose of MMR II was given to a patient.; No further AE details; This spontaneous report was received from other health professional and refers to a 2-year-old female. The patient's medical history, concurrent conditions and concomitant medications were not provided. On 02-AUG-2023, the patient was vaccinated with an expired (expired product administered) measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live recombinant human albumin (rHA) (M-M-R II) subcutaneous injection, 0.5 milliliter, [Lot No. U023829 has been verified to be a valid lot number for [measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (M-M-R II)], expiration date reported as 30-JUL-2023, and confirmed upon internal validation], administered for prophylaxis (strength, and route of administration were not provided). The user of the device (conflicting information as product is not a device) was a repeat user/Health Care Professional, also, it had not been under temperature excursion (TE). The lot number and expiration date for sterile diluent were not provided. No further adverse event (AE) details were provided.