Overview of recall records associated with Flower Orthopedics Corporation, including dates, categories and classifications where available.
Classification mix: Class II: 7.
Device is breaking while in use, potential for patients to require a revision surgery.
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…
Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
Product kit missing CDG 200 (Cannulated Countersink for 3.0-4.5mm Screws) from EWK 201 (Flower E-Kit, Advanced)
This page summarizes recall records in which the official source identifies Flower Orthopedics Corporation as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
