Recall Register

Paragon 28, Inc.: FDA recalls

FDA enforcement reports name Paragon 28, Inc. as the recalling firm in 10 events. The events have 13 product records. The recalls started from 2017 to 2026. All the events are device recalls.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Enforcement events

10 events, newest first.

FDA enforcement events of Paragon 28, Inc.
InitiatedProduct (first record)TypeClassRecordsStatus
10 Jul 2026Custom Made Device Implant 6123 Navicular Cage Small Right Rev A, Model/Catalog Number 6123S R; foot implantDeviceClass III2Ongoing
17 Jun 2026P28 PHANTON INTRAMEDULLARY NAIL SYSTEM, Phantom Hindfoot TTC/TC Ball Tipped Guide Rod, SIZE: 0.30 mm, LENGTH: 800 mmm, ITem number P31-955-1800-S; provides stabilization of the hindfoot and ankle.DeviceClass II1Ongoing
13 Oct 2025Phantom Fibula Nail, 2.8mm x 130mm, Right, Ti, Fibula Nail, REF: P36-128-130R-SDeviceClass II1Ongoing
21 Dec 2023Phantom TTC Nail, 10.0 X 200mm, RightDeviceClass II3Ongoing
13 Jul 2022Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture Anchor SystemDeviceClass II1Ongoing
26 May 2022HammerTube Implant, 2.75mm, 10¿ Cannulated (Sterile)DeviceClass II1Ongoing
18 May 2022Paragon 28, Inc. System: Baby Gorilla/Gorilla Plating System, Ref: P99-100-2816, Material: Stainless Steel; Desc: Drill, 2.4 X 160mmDeviceClass II1Ongoing
30 Jul 2021Phantom Nail System, Drill, 4.6 x 300mm, Cannulated, 3/16" Sq. Connection p28 P99-110-4630DeviceClass II1Terminated
28 Sep 2018P28, Titan 3-D Wedge, Evans, Large, 10 mm, sterile, REF P03-EVN-1010-S, Type: Lagrge, Size: 10mm, (01) 00889795018182, Sterile R, Single Use OnlyDeviceClass II1Terminated
19 Dec 2017P28 JAWS Nitinol Staple System kits are designed for use in an osteotomy, arthrodesis and fragment fixation of bones and joints of the foot including fixation of small bone fragments.DeviceClass II1Terminated

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Type and class

Paragon 28, Inc.: events for each product type
TypeEvents
Device10
Paragon 28, Inc.: events in each class
ClassEvents
Class II9
Class III1
Share of the events of the firm in Class I
0%
Share of all events on the register in Class I
18%
Events with the status Ongoing
7

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of Paragon 28, Inc., by the year that the recall started. The largest year is 2022, with 3 events.

Official channels

Cite this page

Recall Register. Paragon 28, Inc.: FDA recalls. https://recallregister.com/firm/paragon-28-inc/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
State of the firm address
CO

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of Paragon 28, Inc. have?
Class II: 9 events. Class III: 1 event. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of Paragon 28, Inc.?
FDA event 99504, which the firm started on 10 Jul 2026. The first product in the record is: Custom Made Device Implant 6123 Navicular Cage Small Right Rev A, Model/Catalog Number 6123S R; foot implant
How many FDA recalls of Paragon 28, Inc. have the status Ongoing?
7 events have the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.