Recall Z-2081-2021— Mckesson Medical-Surgical Inc. Corporate Office
Class II · Terminated
Class II FDA medical device recall by Mckesson Medical-Surgical Inc. Corporate Office, initiated 2021-06-02, terminated 2022-04-28. FDA's recall record names no specific 510(k) clearance for this event. Product: ANCILLARY ADULT 140-DOSE CONVENIENCE KIT, ITEM #1189482, for the administration of the Moderna COVID-19 vaccine convenience kit for the administration of the COVID-19 vaccine. Reason: Two unsuitable 3mL syringes with conventional needles for vaccine administration included in some Moderna 140 Ancillary Convenience Kits..
- Recalling firm
- Mckesson Medical-Surgical Inc. Corporate Office
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2021-06-02
- Terminated
- 2022-04-28
- Firm location
- Richmond, VA, United States
Product description
ANCILLARY ADULT 140-DOSE CONVENIENCE KIT, ITEM #1189482, for the administration of the Moderna COVID-19 vaccine convenience kit for the administration of the COVID-19 vaccine
Reason for recall
Two unsuitable 3mL syringes with conventional needles for vaccine administration included in some Moderna 140 Ancillary Convenience Kits.
Data sourced from openFDA. This site is unofficial and independent of the FDA.