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Flower Orthopedics Recalls
16 recalls on record · April 1, 2015 to October 18, 2023 · Medical Devices
Recalls by year
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23
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
October 18, 2023Medical DevicesFDA
Flower Orthopedics Corporation recalls Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used to ream and subsequently open the intramedullary
Hazard: Device is breaking while in use, potential for patients to require a revision surgery.
January 12, 2022Medical DevicesFDA
Flower Orthopedics Corporation recalls Flex-Thread Inserter Shaft intended for Fibula intramedullary-intended to be used with the Inserter Draw Rod and Blue R
Hazard: 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 available
October 20, 2021Medical DevicesFDA
Flower Orthopedics Corporation recalls Flower Lag Screw Kit 2.7 mm-intended to be used with 2.7mm lag screws and can be used with any plate that as part of the
Hazard: Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
October 20, 2021Medical DevicesFDA
Flower Orthopedics Corporation recalls 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
Hazard: Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
October 20, 2021Medical DevicesFDA
Flower Orthopedics Corporation recalls Flower Drill Bit Kit 2.4 mm-intended to be used with solid 2.4mm screws and can be used with any plate as part of the Fl
Hazard: Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
October 20, 2021Medical DevicesFDA
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 c
Hazard: Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
October 13, 2021Medical DevicesFDA
Flower Orthopedics Corporation recalls Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201
Hazard: Product kit missing CDG 200 (Cannulated Countersink for 3.0-4.5mm Screws) from EWK 201 (Flower E-Kit, Advanced)
June 9, 2021Medical DevicesFDA
Flower Orthopedics Corporation recalls T25 Cannulated Screwdrivers (CSD 025) packaged in Guide Wire Kits (GWK 300) - Product Usage: Intended to be used to inse
Hazard: Cannulated Screwdrivers may break at the driver tip along the shaft, near the handle extending surgery time and additional x-ray to identify the fragments from the breakages
August 19, 2020Medical DevicesFDA
Flower Orthopedics Corporation recalls Calcaneus Plate, Extensile, Large, Right, Catalog Number CPF 203 - Product Usage: intended to be used for internal fixat
Hazard: The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
August 19, 2020Medical DevicesFDA
Flower Orthopedics Corporation recalls Calcaneus Plate, Extensile, Medium, Right, Catalog Number CPF 202 - Product Usage: intended to be used for internal fixa
Hazard: The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
August 19, 2020Medical DevicesFDA
Flower Orthopedics Corporation recalls Calcaneus Plate, Extensile, Small, Right, Catalog Number CPF 201 - Product Usage: intended to be used for internal fixat
Hazard: The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
August 19, 2020Medical DevicesFDA
Flower Orthopedics Corporation recalls Calcaneus Plate, Extensile, Large, Left, Catalog Number CPF 103 - Product Usage: intended to be used for internal fixati
Hazard: The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
August 19, 2020Medical DevicesFDA
Flower Orthopedics Corporation recalls Calcaneus Plate, Extensile, Medium, Left, Catalog Number CPF 102 - Product Usage: intended to be used for internal fixat
Hazard: The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
August 19, 2020Medical DevicesFDA
Flower Orthopedics Corporation recalls Calcaneus Plate, Extensile, Small, Left, Catalog Number CPF 101 - Product Usage: intended to be used for internal fixati
Hazard: The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
February 8, 2017Medical DevicesFDA
Flower Orthopedics Corporation recalls Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set.
Hazard: The product is being recalled due to incidence and reports of the product breaking during surgery.
April 1, 2015Medical DevicesFDA
Flower Orthopedics Corporation recalls Variable Angle Locking Peg, D:1.8mm x L:14.0mm; Variable Angle Locking Peg, D:1.8mm x L:16.0mm, Variable Angle Locking P
Hazard: Locking pegs were not locking during distal radius procedures. There has been one (1) report of revision surgery scheduled to remove a loosened peg.