MicroMatrix® MM0100FRecalls & reported problems
Acell, Inc. · MicroMatrix® UBM Fine Particulate, 100mg · Class U
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00386190001165), received between Oct 22, 2019 and Oct 22, 2019 — classified as 2 injuries.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (2 reports).
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
- Improper or Incorrect Procedure or Method2
- Off-Label Use2
- Use of Device Problem2
Patient problems
- Chest Pain2
- Fever2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryOct 22, 2019Off-Label Use; Use of Device Problem; Improper or Incorrect Procedure or Method; Off-Label Use; Use of Device Problem; Improper or Incorrect Procedure or Method
ON 9/25/2019 ACELL RECEIVED NOTIFICATION FROM A PHYSICIAN THAT A PATIENT DEVELOPED FEVER AND PLEURISY LIKE SYMPTOMS (CHEST AND BACK PAIN) AFTER A HAIR RESTORATION PROCEDURE WITH MICROMATRIX, PLASMALYTE AND PLATELET RICH PLASMA (PRP). THE PROCEDURE WAS DONE ON (B)(6) 2019 AND THE PATIENT DEVELOPED THE AFOREMENTIONED SYMPTOMS ON THE SAME DAY. THERE HAS NOT BEEN ANY TREATMENT ADVISED TO THE PATIENT OR MEDICAL INTERVENTION POST INCIDENT.
Patient problems: Chest Pain; Fever
MAUDE report 9218567 ↗InjuryOct 22, 2019Off-Label Use; Use of Device Problem; Improper or Incorrect Procedure or Method; Off-Label Use; Use of Device Problem; Improper or Incorrect Procedure or Method
ON (B)(6) 2019 ACELL RECEIVED NOTIFICATION FROM A PHYSICIAN THAT A PATIENT DEVELOPED FEVER AND PLEURISY LIKE SYMPTOMS (CHEST AND BACK PAIN) AFTER A HAIR RESTORATION PROCEDURE WITH MICROMATRIX, PLASMALYTE AND PLATELET RICH PLASMA (PRP). THE PROCEDURE WAS DONE ON (B)(6) 2019 AND THE PATIENT DEVELOPED THE AFOREMENTIONED SYMPTOMS ON THE SAME DAY. THERE HAS NOT BEEN ANY TREATMENT ADVISED TO THE PATIENT OR MEDICAL INTERVENTION POST INCIDENT.
Patient problems: Chest Pain; Fever
MAUDE report 9218566 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.