Flower Drill Bit Kit 2 — Class II medical device recall Z-0111-2022
Terminated recall by Flower Orthopedics Corporation, reported 2021-10-20, distributed in AZ, CA, CO, FL, IL, IN, NV, OH…. Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
| Recall number | Z-0111-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Flower Orthopedics Corporation, Horsham, PA, United States |
| Recall initiated | 2021-09-01 |
| Classified | 2021-10-13 |
| Reported by FDA | 2021-10-20 |
| Terminated | 2023-02-16 |
| Distributed | AZ, CA, CO, FL, IL, IN, NV, OH, TX, VA |
| Quantity | 2 units |
| UPC / GTIN / UDI-DI | 00840118101264 |
| Lot numbers | 2013002721, 2013003589 |
| Model numbers | 020, 2013002721 |
Product
Flower Drill Bit Kit 2.0 mm - intended to be used with solid 2.0mm screws and can be used with any plate that has been cleared as part of the Flower Small and Medium Implant Set and uses the small locking mechanism. mechanism. Catalog Number: DBK 020 2013002721
Reason for recall
Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
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-0111-2022. 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.