ANCILLARY ADULT 140-DOSE CONVENIENCE KIT — Class II medical device recall Z-2081-2021
Terminated recall by Mckesson Medical-Surgical Inc. Corporate Office, reported 2021-07-28, distributed nationwide. Two unsuitable 3mL syringes with conventional needles for vaccine administration included in some Moderna 140
| Recall number | Z-2081-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mckesson Medical-Surgical Inc. Corporate Office, Richmond, VA, United States |
| Recall initiated | 2021-06-02 |
| Classified | 2021-07-16 |
| Reported by FDA | 2021-07-28 |
| Terminated | 2022-04-28 |
| Distributed | Nationwide (US) |
| Quantity | 53,388 kits |
| Lot numbers | 0296288, 0324761, 0324763, 0324766, 0324770, 1015383, 1020431, 9252960, 9252961 |
| Model numbers | 1189482 |
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 for recall
Two unsuitable 3mL syringes with conventional needles for vaccine administration included in some Moderna 140 Ancillary Convenience Kits.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2081-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.