ALLEN 104002Recalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00615521004125), received between Aug 5, 2022 and May 19, 2026 — classified as 1 injury, 7 malfunctions.

The most frequently reported specific device problem is “Fracture” (6 reports).

1 FDA recall record name this device's identifier.

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 16, 2026.

Recalls naming this device

1. Sep 20, 2022Terminated

   the adhesive, applied to screws and bolts as an additional holding force, may not cure correctly, and as a result, could result in a loss of holding and reduced mechanical integrity.

   Z-0179-2023 · Root cause: Other · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 19, 2026Fracture

  A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT ALLEN LIFT ASSIST BEACH CHAIR HAD AN ISSUE, CRACKED FIBER BOARD. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25217788 ↗
• MalfunctionMay 19, 2026Fracture

  A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT ALLEN LIFT ASSIST BEACH CHAIR HAD AN ISSUE, CRACKED FIBER BOARD. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25217787 ↗
• MalfunctionApr 24, 2026Fracture

  A DISTRIBUTOR CONTACTED TECHNICAL SERVICE TO REPORT THAT BCH CHR POSITION BEACH CHAIR'S BACK PLATE WAS CRACKED. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24982339 ↗
• MalfunctionMar 9, 2026Fracture

  BAXTER RECEIVED A REPORT STATING THAT ALLEN LIFT ASSIST BEACH CHAIR BACKBOARD WAS CRACKED. THE BED WAS LOCATED AT THE ACCOUNT AND OCCURRED AFTER PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24553291 ↗
• InjuryJun 24, 2025Fracture; Fracture

  IT WAS REPORTED A ALLEN LIFT ASSIST BEACH CHAIR EXTENSION ¿GAVE WAY¿ AND THE PATIENT FELL. THE PATIENT WAS ADMITTED TO THE HOSPITAL FOR AN EMERGENCY LEFT ACROMIOCLAVICULAR (AC) JOINT SEPARATION PROCEDURE. THE PATIENT WAS INTUBATED AND SEDATED. PRIOR TO THE END OF THE PROCEDURE, THE MEDICAL STAFF WERE ADJUSTING THE TABLE EXTENSION AND THE TABLE EXTENSION ¿GAVE WAY.¿ THE PATIENT STARTED FALLING HEADFIRST; HOWEVER, THE SURGEON AND NURSES WERE ABLE TO ¿PARTIALLY CONTROLLED THE FALL.¿ THE PATIENT DID END UP FALLING AND HITTING THEIR HEAD. THE PATIENT SUSTAINED A ¿SMALL LACERATION¿ TO THEIR HEAD. THE ENDOTRACHEAL TUBE REMAINED INTACT, AND THE PATIENT REMAINED HEMODYNAMICALLY STABLE. THE MEDICAL EMERGENCY TEAM (MET) WERE CALLED TO HAVE ADDITIONAL STAFF TO ASSIST IN THE SURGICAL THEATER. SPINAL PRECAUTION PROTOCOLS WERE PUT IN PLACE AND THE TEAM WAS ABLE TO SAFELY RETURN THE PATIENT TO THE TABLE. THE PATIENT REMAINED INTUBATED AND WAS TRANSFERRED TO RADIOLOGY FOR AN URGENT COMPUTED TOMOGRAPHY SCAN (CT) BRAIN AND NECK. CT RESULTS WERE CLEAR. THE PATIENT REMAINED IN FULL SPINAL PRECAUTIONS OVERNIGHT UNTIL A FULL TERTIARY SURVEY COULD BE COMPLETED. THE FOLLOWING DAY, THE PATIENT WAS CLEARED A

  Patient problems: Laceration(s)

  MAUDE report 22321227 ↗
• MalfunctionMar 11, 2025Fracture; Fracture

  BAXTER RECEIVED A REPORT STATING THAT ALLEN LIFT ASSIST BEACH CHAIR BACKBOARD WERE CRACKED AND WAS RECLINING SLIGHTLY. THE BED WAS LOCATED AT THE ACCOUNT AND OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY, NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21577125 ↗
• MalfunctionJun 6, 2023Mechanical Problem; Mechanical Problem

  THE CUSTOMER INITIALLY REPORTED THAT THE BEACH CHAIR'S SUPPORT BROKE DURING SURGERY. THERE WAS NO ALLEGATION OF PATIENT OR CAREGIVER INJURY AS A RESULT OF THIS EVENT. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17072908 ↗
• MalfunctionAug 5, 2022Mechanical Problem; Mechanical Problem

  IT WAS REPORTED THE STRUT COMPONENT OF A BEACH CHAIR DEVICE WAS NOT HOLDING DURING USE RESULTING IN A PROCEDURE DELAY FOR PATIENT TRANSFER TO ANOTHER DEVICE. NO ALLEGED INJURY, OCCURRED. THIS EVENT WAS CAPTURED UNDER HILLROM COMPLAINT REF # (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15175813 ↗