Battalion 27428Recalls & reported problems

Alphatec Spine, Inc. · BATTALION, LLIF TABLE FIXATION ARM, BLUE · Class 1

Adverse event reports: 3
Deaths reported: 0
Injuries reported: 3
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00840967129136), received between Apr 10, 2019 and Oct 26, 2020 — classified as 3 injuries.

The most frequently reported specific device problem is “Break” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

Break1
Failure to Disconnect1
Physical Resistance/Sticking1

Patient problems

Insufficient Information1
No Clinical Signs, Symptoms or Conditions1
No Code Available1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

InjuryOct 26, 2020Failure to Disconnect
RETRACTOR ARM BUTTON WOULD NOT RELEASE FROM RETRACTOR. THE EVENT CAUSED JUST OVER A 30 MINUTE DELAY IN THE CASE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10737511 ↗
InjurySep 13, 2020Physical Resistance/Sticking
RETRACTOR ARM BUTTON BECAME STUCK AND WOULD NOT RELEASE FROM RETRACTOR. THE EVENT CAUSED JUST OVER A 30 MINUTE DELAY IN THE CASE.
Patient problems: Insufficient Information
MAUDE report 10526172 ↗
InjuryApr 10, 2019Break
WHILE STARTING THE LATERAL PROCEDURE, ATTEMPTED TO PLACE RETRACTOR AND NOTED ON THE BACK TABLE THAT THE DOCKING ARM/LOCKING MECHANISM ON RETRACTOR ARM HAD DISASSEMBLED AND COULD NOT BE REASSEMBLED. THE GOLD BUTTON ON THE TABLE FIXATION ARM WAS NOT FUNCTIONING. PATIENT WAS ON THE TABLE WITH AN INCISION AND DILATORS PLACED. SURGERY HAD TO BE RESCHEDULED. THE EVENT CAUSED OVER A 30 MINUTE DELAY IN THE CASE.
Patient problems: No Code Available
MAUDE report 8499649 ↗

Device details

UDI-DI	`00840967129136`
Brand	Battalion
Model	27428
Company	Alphatec Spine, Inc.
Product code	CCX · SUPPORT, PATIENT POSITION
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	Not in Commercial Distribution
Record updated	Feb 6, 2025

Device type (GMDN): Operating table orthopaedic extension, non-powered

A non-powered, orthopaedic device intended to function as a freestanding framework or that can be attached to an operating table or table top to provide additional support to a patient's body segment or part during orthopaedic surgical procedures (e.g., lower trunk for traction of the legs, upper body during shoulder or spinal surgery, C- or O-arm use). It typically consists of height, length and angle adjustable supports or telescopic bars/plates (e.g., leg spar).

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.