Flower Drill Bit Kit 2 — Class II medical device recall Z-0113-2022
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-0113-2022 |
|---|---|
| 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 | 3 units |
| UPC / GTIN / UDI-DI | 00840118101295 |
| Lot numbers | 2013003588, 2013004613 |
| Model numbers | 027 |
Product
Flower Drill Bit Kit 2.7mm- The Drill Bit Kit, 2.7mm (DBK 027) is intended to be used with solid 2.7mm screws and can be used with any the Flower Small and Medium Implant Set Flower Ankle Plating Set , Flower Rear Foot/Calcaneus Plating Set or Flower Upper Extremity Plating Set and uses the medium locking mechanism. Catalog Number: DBK 027
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-0113-2022. 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.