MicroMatrix® MM0200Recalls & reported problems
Acell, Inc. · MicroMatrix® UBM Standard Particulate, 200mg · Class U
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00386190001172), received between Jan 6, 2020 and Jan 6, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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
- Improper or Incorrect Procedure or Method1
- Off-Label Use1
- Use of Device Problem1
Patient problems
- Swelling1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 6, 2020Off-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 12/10/2019 ACELL RECEIVED NOTIFICATION FROM A PHYSICIAN THAT A PATIENT DEVELOPED SWELLING OF THE EYES AFTER A HAIR RESTORATION PROCEDURE WHICH INVOLVED SCALP INJECTIONS WITH MICROMATRIX RECONSTITUTED WITH PLATELET RICH PLASMA (PRP). THE PROCEDURE WAS CONDUCTED ON (B)(6) 2019. THE ONSET DATE OF THE PATIENT'S ADVERSE REACTION IS (B)(6) 2019. AS A PRECAUTIONARY MEASURE, PHYSICIAN PRESCRIBED A COURSE OF STEROIDS (MEDROL PACK). ACELL HAS REASON TO SUSPECT THAT THE PATIENT ALSO RECEIVED AN ADDITIONAL COSMETIC PROCEDURE AT THE TIME OF THE HAIR RESTORATION PROCEDURE BECAUSE SURGEON'S COMMENT ABOUT THE PATIENT NEEDING TO COME IN FOR SUTURE REMOVAL.
Patient problems: Swelling
MAUDE report 9555791 ↗
Other DRESSING, WOUND, COLLAGEN devices
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- Cytal® BMM0710Acell, Inc. · DRESSING, WOUND, COLLAGEN1 recall0 reports
- Cytal® WSM0710Acell, Inc. · DRESSING, WOUND, COLLAGEN1 recall0 reports
- PriMatrix® 607-001-125Tei Biosciences Inc. · DRESSING, WOUND, COLLAGEN1 recall0 reports
- DermaCol 100 00300ESion Brands LLC · Dressing, Wound, Collagen1 recall0 reports
- DermaCol 100 00300ESion Brands LLC · Dressing, Wound, Collagen1 recall0 reports
- PriMatrix® 607-004-880Tei Biosciences Inc. · DRESSING, WOUND, COLLAGEN1 recall0 reports
- GIBSON HEALTHCARE 5251-194Benco Dental Supply CO. · Dressing, Wound, Collagen1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.