Flower Orthopedics Corporation recalls
Every recall we track for Flower Orthopedics Corporation — 14 in all, from 2020–2023 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Flower Orthopedics Corporation peaked in 2021 (7); 14 since 2017.
All FDA recall records for Flower Orthopedics Corporation since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 6 | 0 | 6 |
| 2021 | 0 | 2 | 5 | 0 | 7 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 1 | 0 | 0 | 1 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Flower Orthopedics Corporation product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Flower Orthopedics Corporation recalls
6 shown- Use cautionMedical device
Flower Orthopedics Corporation recalls Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used to ream and subsequently open the
Flower Orthopedics recalls 3.2mm Flex-Thread Reamers that may break during use, potentially requiring revision surgery. Affected units have specific catalog and lot numbers.
Flower OrthopedicsAug 29, 2023 - Use cautionMedical device
Flower Orthopedics Corporation recalls Flex-Thread Inserter Shaft intended for Fibula intramedullary-intended to be used with the Inserter Draw Rod and Blue
Flower Orthopedics recalls Flex-Thread Inserter Shaft for fibula intramedullary use due to incompatibility with Inserter Draw Rod causing binding during surgery. Affected units have specific catalog and lot numbers.
Flower OrthopedicsNov 2, 2021 - Lower riskMedical device
Flower Orthopedics Corporation recalls Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201
Flower Orthopedics recalls EWK 201 bone fixation kit missing CDG 200 component. This could lead to improper bone fixation. Affected units sold with lot number 2104321637.
Flower OrthopedicsSep 3, 2021 - Lower riskMedical device
Flower Orthopedics Corporation recalls 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
Flower Orthopedics recalls 2.0mm drill bit kits missing AO connect feature, which could delay surgical procedures. Affected kits have specific catalog and lot numbers.
Flower OrthopedicsSep 1, 2021 - Use cautionMedical device
Flower Orthopedics Corporation recalls T25 Cannulated Screwdrivers (CSD 025) packaged in Guide Wire Kits (GWK 300) - Product Usage: Intended to be used to
Flower Orthopedics recalls T25 Cannulated Screwdrivers (CSD 025) in Guide Wire Kits (GWK 300) that may break during surgery, causing longer procedures and additional x-rays. Affected units have specific lot numbers.
Flower OrthopedicsApr 15, 2021 - Lower riskMedical device
Flower Orthopedics Corporation recalls Calcaneus Plate, Extensile, Medium, Left, Catalog Number CPF 102 - Product Usage: intended to be used for internal
Flower Orthopedics recalls specific calcaneus plates made with incorrect titanium alloy. This may cause complications during bone repair. Affected units include catalog number CPF 102, lot numbers 1909660029 and 1909660031.
Flower OrthopedicsJul 8, 2020
Flower Orthopedics Corporation recall questions
How many recalls has Flower Orthopedics Corporation had?
14 recalls from Flower Orthopedics Corporation are on record with U.S. safety agencies, from 2020–2023.
What is the most recent Flower Orthopedics Corporation recall?
Flower Orthopedics Corporation recalls Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used to ream and subsequently open the, dated Aug 29, 2023. Every Flower Orthopedics Corporation recall is listed on this page, newest first.
What should I do if I have a recalled Flower Orthopedics Corporation product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Flower Orthopedics Corporation recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.