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Report #2885844

Received Feb 17, 2026

A note on interpretation. VAERS reports are unverified and may be incomplete or coincidental. A report does not establish that a vaccine caused an event, and counts should not be used to calculate incidence or infer causation. Full disclaimer

Overview

Sex
Unknown
Age
Age unknown
State
ID
Recovered
Unknown
Vaccinated
Onset
Days to onset
Hospital days

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
RSVRSV (ABRYSVO)PFIZER\WYETH1MN0308

Symptoms (1)

Product container issue

Symptom narrative

Glass vials shattered and cut the nurse; one of them the glass vials actually shattered and actually cut the nurse.; one of them the glass vials actually shattered and actually cut the nurse.; This is a spontaneous report received from a Nurse from product quality group. A patient (age and gender not provided) received rsv vaccine prot.subunit pref 2v (ABRYSVO), as dose 1, single (Lot number: MN0308, Expiration Date: 31Oct2026) for immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: INJURY (non-serious), outcome "unknown", described as "Glass vials shattered and cut the nurse"; OCCUPATIONAL EXPOSURE TO PRODUCT (non-serious), PRODUCT CONTAINER ISSUE (non-serious), outcome "unknown" and all described as "one of them the glass vials actually shattered and actually cut the nurse.". Additional information: Pfizer employee stated, basically some Act-O-Vial of Abrysvo malfunctioned, there are 5 of them. In four of them the plunger would not disengage and in one of them the glass vials actually shattered and actually cut the nurse. There are five separate vials. Pfizer employee stated, So, the first vial is, Lot# MN0308. Pfizer employee stated, Yes, they told that they have either one or two. One of them shattered so obviously they do not have that one. Packaging sealed and intact. Pfizer employee stated, MN0304, MM9167, and that one, MM9167. They said that they have that vial to return. When probed if the defective Abrysvo administered to the patient, Pfizer employee does not thought any of them have, no. Looks like, just when Pfizer employee had the work. Follow-up (10Feb2026): This is a follow-up report combining information from duplicate reports 202600027229 and 202600027030. The current and all subsequent information will be reported under manufacturer report number 202600027030. The new information reported from a Nurse includes: Reporter details, Lot and expiry date captured.