LIF-PTP 300-351Recalls & reported problems
Alphatec Spine, Inc. · Keyed Bedrail Clamp · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00190376307169), received between Jul 15, 2021 and Jul 15, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device-Device Incompatibility” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Device-Device Incompatibility1
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 15, 2021Mechanical Problem; Device-Device Incompatibility
DURING THE PTP PORTION OF THE PROCEDURE, THE A-ARM WAS INCAPABLE OF LOADING INTO THE BEDRAIL CLAMP, CAUSING A DELAY IN THE CASE. A LIF CLAMP WAS ABLE TO BE UNITIZED WHICH ALLOWED THE CASE TO PROCEED. NO PATIENT INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12174351 ↗
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- Battalion 27428Alphatec Spine, Inc. · SUPPORT, PATIENT POSITION3 reports
- ACUFEX 72205103Smith & Nephew, Inc. · SUPPORT, PATIENT POSITION2 reports
- Medline MSC50023Medline Industries, Inc. · SUPPORT, PATIENT POSITION2 reports
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- Olympic Vac-Pac Size 30Natus Medical Incorporated · Support, Patient Position2 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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