ALLEN 107003 (REF A-71100-US)Recalls & reported problems

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00615521003012), received between Oct 7, 2022 and Aug 11, 2026 — classified as 3 injuries, 6 malfunctions.

The most frequently reported specific device problem is “Unintended Movement” (5 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. How this data works · Data updated Oct 13, 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-0175-2023 · Root cause: Other · FDA record ↗

Most reported problems

Recent adverse event reports

The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 11, 2026Unintended Movement

  Baxter received a report that ALLEN ADVANCE TABLE US had brakes not holding. There was no patient/user injury, medical intervention, symptom, or adverse event reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50216849 ↗
• MalfunctionApr 9, 2026Detachment of Device or Device Component

  BAXTER RECEIVED A REPORT STATING THAT WHEN THE ALLEN ADVANCE TABLE WAS FLIPPED, THE ALLEN SUPINE ACCESS TOP ACCESSORY FELL OFF OF THE TABLE DURING AN IN-SERVICE INSPECTION. THE SURGICAL TABLE WAS LOCATED AT THE ACCOUNT AND OCCURRED BEFORE 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 24831827 ↗
• MalfunctionMay 29, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT STATING THAT ALLEN ADVANCE TABLE BRAKE CASTERS WERE SWIVELING WHILE BRAKES WERE ENGAGED. THE BED WAS LOCATED AT THE ACCOUNT AND OCCURRED DURING BAXTER SERVICING/TESTING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22107833 ↗
• MalfunctionMay 26, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT STATING THAT ALLEN ADVANCE TABLE BRAKE CASTERS WERE SWIVELING WHILE BRAKES WERE ENGAGED. THE BED WAS LOCATED AT THE ACCOUNT AND OCCURRED DURING BAXTER SERVICING/TESTING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22084899 ↗
• MalfunctionMar 24, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT STATING THAT ALLEN ADVANCE TABLE US CASTERS WERE NOT HOLDING WHEN LOCKED. THE TABLE WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21678437 ↗
• MalfunctionMar 11, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT STATING THAT ALLEN ADVANCE TABLE CASTERS WERE NOT HOLDING BRAKE WHEN BEING LOCKED. THE TABLE WAS LOCATED AT THE ACCOUNT AND OCCURRED DURING BIOMED TESTING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21575267 ↗
• InjuryOct 11, 2022Positioning Problem; Positioning Problem

  IT WAS REPORTED THAT THREE PATIENTS DEVELOPED POST-OPERATIVE FEMORAL CUTANEOUS NERVE PALSY RELATED TO POSITIONING ON THE ALLEN TABLE. THE CUSTOMER NOTES THE FOLLOWING FOR ALL THREE PATIENTS: DIAGNOSIS OF LUMBER RADICULOPATHY, SURGICAL PRONE POSITION WITH CHEST, HIP, AND THIGH PADS, SIGNS AND SYMPTOMS OF POST-OP NERVE PALSY INCLUDING NUMBNESS AND DYSESTHESIA OF THE RIGHT THIGH, WITH ONE HAVING BILATERAL NUMBNESS AND DYSESTHESIA. NO MEDICAL INTERVENTION REQUIRED, AND FINAL PATIENT OUTCOME IS ONGOING. FOLLOW-UP ATTEMPTS WERE MADE WITH THE CUSTOMER, HOWEVER, THEY HAVE NOT PROVIDED ANY FURTHER DETAILS INCLUDING DEVICE SERIAL NUMBERS ASSOCIATED WITH EACH PATIENT, IF THE CORRECT SIZE OR TABLE PADS WERE USED AND PLACED CORRECTLY, AND IF THE CORRECT SIZE ARM BOARD CLAMPS USED WITH THE DEVICE WERE SET AT APPROPRIATE HEIGHTS. THE THREE PATIENTS WILL BE ASSESSED SEPARATELY IN THE FOLLOWING (B)(6). THIS REPORT REFERENCES PATIENT 3. PATIENT 3 HAD RIGHT L3/4, L4/5 AND L5/S1 LAMINOTOMIES, LASTING 6.5 HOURS. DAY ONE POST-OP THE NERVE PALSY WAS NOTED. THIS EVENT WAS CAPTURED UNDER HILL-ROM COMPLAINT REF #(B)(4).

  Patient problems: Nerve Damage; Numbness

  MAUDE report 15576520 ↗
• InjuryOct 10, 2022Positioning Problem; Positioning Problem

  IT WAS REPORTED THAT THREE PATIENTS DEVELOPED POST-OPERATIVE FEMORAL CUTANEOUS NERVE PALSY RELATED TO POSITIONING ON THE ALLEN TABLE. THE CUSTOMER NOTES THE FOLLOWING FOR ALL THREE PATIENTS: DIAGNOSIS OF LUMBER RADICULOPATHY, SURGICAL PRONE POSITION WITH CHEST, HIP, AND THIGH PADS, SIGNS AND SYMPTOMS OF POST-OP NERVE PALSY INCLUDING NUMBNESS AND DYSESTHESIA OF THE RIGHT THIGH, WITH ONE HAVING BILATERAL NUMBNESS AND DYSESTHESIA. NO MEDICAL INTERVENTION REQUIRED, AND FINAL PATIENT OUTCOME IS ONGOING. FOLLOW-UP ATTEMPTS WERE MADE WITH THE CUSTOMER, HOWEVER, THEY HAVE NOT PROVIDED ANY FURTHER DETAILS INCLUDING DEVICE SERIAL NUMBERS ASSOCIATED WITH EACH PATIENT, IF THE CORRECT SIZE OR TABLE PADS WERE USED AND PLACED CORRECTLY, AND IF THE CORRECT SIZE ARM BOARD CLAMPS USED WITH THE DEVICE WERE SET AT APPROPRIATE HEIGHTS. THE THREE PATIENTS WILL BE ASSESSED SEPARATELY IN THE FOLLOWING, (B)(6)(PATIENT 1), (B)(6) (PATIENT 2), (B)(6)(PATIENT 3) THIS REPORT REFERENCES PATIENT 2. PATIENT 2 HAD AN L4 - S1 POSTERIOR SPINAL FUSION (PSF), LASTING 6.5 HOURS. DAY ONE POST-OP THE NERVE PALSY WAS NOTED. THIS EVENT WAS CAPTURED UNDER HILL-ROM COMPLAINT REF # (B)(4).

  Patient problems: Nerve Damage; Numbness

  MAUDE report 15570841 ↗
• InjuryOct 7, 2022Positioning Problem; Positioning Problem

  IT WAS REPORTED THAT THREE PATIENTS DEVELOPED POST-OPERATIVE FEMORAL CUTANEOUS NERVE PALSY RELATED TO POSITIONING ON THE ALLEN TABLE. THE CUSTOMER NOTES THE FOLLOWING FOR ALL THREE PATIENTS: DIAGNOSIS OF LUMBER RADICULOPATHY, SURGICAL PRONE POSITION WITH CHEST, HIP, AND THIGH PADS, SIGNS AND SYMPTOMS OF POST-OP NERVE PALSY INCLUDING NUMBNESS AND DYSESTHESIA OF THE RIGHT THIGH, WITH ONE HAVING BILATERAL NUMBNESS AND DYSESTHESIA. NO MEDICAL INTERVENTION REQUIRED, AND FINAL PATIENT OUTCOME IS ONGOING. FOLLOW-UP ATTEMPTS WERE MADE WITH THE CUSTOMER, HOWEVER, THEY HAVE NOT PROVIDED ANY FURTHER DETAILS INCLUDING DEVICE SERIAL NUMBERS ASSOCIATED WITH EACH PATIENT, IF THE CORRECT SIZE OR TABLE PADS WERE USED AND PLACED CORRECTLY, AND IF THE CORRECT SIZE ARM BOARD CLAMPS USED WITH THE DEVICE WERE SET AT APPROPRIATE HEIGHTS. THE THREE PATIENTS WILL BE ASSESSED SEPARATELY IN THE FOLLOWING (B)(6). THIS REPORT REFERENCES PATIENT 1 PATIENT 1 HAD AN L4 - S1 POSTERIOR SPINAL FUSION (PSF), LASTING 6.5 HOURS. DAY ONE POST-OP THE NERVE PALSY WAS NOTED. THIS EVENT WAS CAPTURED UNDER HILL-ROM COMPLAINT REF # (B)(4).

  Patient problems: Nerve Damage; Numbness

  MAUDE report 15561081 ↗