Flower Orthopedics recalls
4 official recalls and safety alerts involving Flower Orthopedics since 2021-10, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Flower Orthopedics or the relevant agency.
- 2023-10-18
USFlower Orthopedics Corporation recalls Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used to ream and subsequently open the intramedullary canal to…
Device is breaking while in use, potential for patients to require a revision surgery.
- 2022-01-12
- US
Flower Orthopedics Corporation recalls Flex-Thread Inserter Shaft intended for Fibula intramedullary-intended to be used with the Inserter Draw Rod and Blue Ratchet…
Mating incompatibility between the Inserter Shaft and the Inserter Draw Rod causing the inserter draw rod to bind and not rotate freely as intended surgeon may be unable to complete surgery unless a second set is…
FDA · DeviceFlower Orthopedics CorporationUS Nationwide distribution in the states of AZ, CA, CO, GA, TN, FL, IL, MA,…Official notice → - 2021-10-20
- US
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 cleared as…
Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
FDA · DeviceFlower Orthopedics CorporationArizona California Colorado Florida Florida Illinois Indiana Nevada Ohio Texas…Official notice → - 2021-10-13
- US
Flower Orthopedics Corporation recalls Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201
Product kit missing CDG 200 (Cannulated Countersink for 3.0-4.5mm Screws) from EWK 201 (Flower E-Kit, Advanced)
FDA · DeviceFlower Orthopedics CorporationUS Nationwide distribution in the states of AZ, CA, CO,CT, FL, IL, IN, NC, NY,…Official notice →