Device recall: AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous…

Class II FDA enforcement event 87677. Recall start date: 29 Mar 2021. Status in the FDA record: Terminated. Termination date: 27 Apr 2023.

Reason for recall, in the words of FDA

3/4 AFT Straight Fill Tubes (227007) filled only 1/2 way instead of 3/4, may cause delay of surgery

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

Musculoskeletal Transplant Foundation, Inc. started this device recall on 29 Mar 2021. The firm address in the FDA record is in Edison, NJ. FDA put the recall in Class II. FDA event 87677 has 1 product record. The first FDA enforcement report date is 19 May 2021. The record gives the status Terminated, with the termination date 27 Apr 2023.

FDA enforcement report The 1 product record

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 1 Oct 2026. openFDA export of 28 Sep 2026.

Distribution

In the words of FDA.

US Nationwide distribution in the state of MN.

Recalling firm

Musculoskeletal Transplant Foundation, Inc., Edison, NJ.

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

FDA records how the recall started: Voluntary: Firm initiated.

Products

1 product record in the event.

FDA event 87677: product records
Recall number	Product	Quantity	Class	Status	Report date
Z-1562-2021	AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous defects created from traumatic injury. It can be used in the: extremities, pelvis, and spine Item Number: 227007	672 units	Class II	Terminated	19 May 2021

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.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

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

Class II: The middle of the three FDA recall classes.

The event in context

Device events that started in 2021: 900
Share of these events in Class II: 89%
Product records in this event: 1Median of the firm: 1
Events of the firm on the register: 8

Other events of the firm

Other FDA enforcement events of Musculoskeletal Transplant Foundation, Inc.
Initiated	Product (first record)	Type	Class	Records
22 Dec 2023	AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)	Device	Class II	2
22 Sep 2023	DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defect	Device	Class II	1
15 Aug 2019	QuickGraft Model # 430PST	Device	Class II	1
21 Apr 2016	Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treatment of surgically-created oss	Device	Class II	1
27 May 2015	Cortical Pin 2.0 mm,Sterile, FREEZE DRIED: Store at ambient temperature. Do Not freeze.	Device	Class II	1
27 May 2015	Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical Instruments are designed for the specific needs	Device	Class II	1
4 Dec 2014	DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void filler.	Device	Class II	1

Musculoskeletal Transplant Foundation, Inc.: all 8 events

Official channels

FDA enforcement report Z-1562-2021The FDA record of the first product of this event.
FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
FDA MedWatchThe FDA safety reporting program for drugs and medical devices.

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Cite this page

Recall Register. FDA enforcement event 87677. https://recallregister.com/fda/ii/87677/. Source: openFDA enforcement reports. Data through 28 Sep 2026.

Sources

Source: openFDA device enforcement reports
Licence: CC0 1.0
Export date: 28 Sep 2026
Newest FDA report date on the register: 23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?: The FDA record gives this distribution: US Nationwide distribution in the state of MN.
What quantity of product is in FDA event 87677?: The FDA record gives this quantity: 672 units
How did the recall start?: The FDA record says: Voluntary: Firm initiated
How many device recalls of 2021 have the same class?: 89% of the 900 device events that started in 2021 are in Class II.