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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 84334

6 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
November 05, 2019
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Collagen Matrix Inc

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

6 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 6

GIBSON Healthcare Membrane 6-9, 15mm x 20mm, Reference Number 5303-226 - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets; localized ridge augmentation for later implantation; alveolar ridge reconstruction for prosthetic treatment; filling of bone defects; guided bone regeneration in dehiscence defects and guided tissue regeneration procedures in periodontal defects.

Z-0907-2020
Recall number
Z-0907-2020
Initiated
November 05, 2019
Classification
Class II
Status
Terminated
Recalling firm
Collagen Matrix Inc
Quantity
192 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products may have been packaged with an incorrect Instructions for Use.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The products may have been packaged with an incorrect Instructions for Use.

Code information

UDI: (01)00366975013248(17)200630; Lot Number PDMU18F1, PDMU19A1

Distribution pattern

US Nationwide distribution in the states of AR, AZ, CA, CO, FL, IL, MA, MD, MI, MN, NC, NJ, NY, OK, PA, SC, TX, UT, VA, and WA.

device · product 2 of 6

GIBSON Healthcare Membrane 6-9, 20mm x 30mm, Reference Number 5303-235 - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets; localized ridge augmentation for later implantation; alveolar ridge reconstruction for prosthetic treatment; filling of bone defects; guided bone regeneration in dehiscence defects and guided tissue regeneration procedures in periodontal defects.

Z-0908-2020
Recall number
Z-0908-2020
Initiated
November 05, 2019
Classification
Class II
Status
Terminated
Recalling firm
Collagen Matrix Inc
Quantity
192 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products may have been packaged with an incorrect Instructions for Use.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The products may have been packaged with an incorrect Instructions for Use.

Code information

UDI: (01)00366975013255(17)200630; Lot Number PDMU18F1

Distribution pattern

US Nationwide distribution in the states of AR, AZ, CA, CO, FL, IL, MA, MD, MI, MN, NC, NJ, NY, OK, PA, SC, TX, UT, VA, and WA.

device · product 3 of 6

GIBSON Healthcare Membrane 6-9, 30mm x 40mm, Reference Number 5303-299 - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets; localized ridge augmentation for later implantation; alveolar ridge reconstruction for prosthetic treatment; filling of bone defects; guided bone regeneration in dehiscence defects and guided tissue regeneration procedures in periodontal defects.

Z-0909-2020
Recall number
Z-0909-2020
Initiated
November 05, 2019
Classification
Class II
Status
Terminated
Recalling firm
Collagen Matrix Inc
Quantity
192 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products may have been packaged with an incorrect Instructions for Use.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The products may have been packaged with an incorrect Instructions for Use.

Code information

UDI: (01)00366975013255(17)210531; Lot Number PDMU19C1

Distribution pattern

US Nationwide distribution in the states of AR, AZ, CA, CO, FL, IL, MA, MD, MI, MN, NC, NJ, NY, OK, PA, SC, TX, UT, VA, and WA.

device · product 4 of 6

GIBSON Healthcare Membrane Extended, 15mm x 20mm, Reference Number 5303-306 - - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets; localized ridge augmentation for later implantation; alveolar ridge reconstruction for prosthetic treatment; filling of bone defects; guided bone regeneration in dehiscence defects and guided tissue regeneration procedures in periodontal defects.

Z-0910-2020
Recall number
Z-0910-2020
Initiated
November 05, 2019
Classification
Class II
Status
Terminated
Recalling firm
Collagen Matrix Inc
Quantity
192 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products may have been packaged with an incorrect Instructions for Use.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The products may have been packaged with an incorrect Instructions for Use.

Code information

UDI: (01)00366975013279(17)200630; Lot Number EPDMU18H1

Distribution pattern

US Nationwide distribution in the states of AR, AZ, CA, CO, FL, IL, MA, MD, MI, MN, NC, NJ, NY, OK, PA, SC, TX, UT, VA, and WA.

device · product 5 of 6

GIBSON Healthcare Membrane Extended, 20mm x 30mm, Reference Number 5303-324 - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets; localized ridge augmentation for later implantation; alveolar ridge reconstruction for prosthetic treatment; filling of bone defects; guided bone regeneration in dehiscence defects and guided tissue regeneration procedures in periodontal defects.

Z-0911-2020
Recall number
Z-0911-2020
Initiated
November 05, 2019
Classification
Class II
Status
Terminated
Recalling firm
Collagen Matrix Inc
Quantity
192 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products may have been packaged with an incorrect Instructions for Use.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The products may have been packaged with an incorrect Instructions for Use.

Code information

UDI: (01)00366975013286(17)200630; Lot Number EPDMU18H1

Distribution pattern

US Nationwide distribution in the states of AR, AZ, CA, CO, FL, IL, MA, MD, MI, MN, NC, NJ, NY, OK, PA, SC, TX, UT, VA, and WA.

device · product 6 of 6

GIBSON Healthcare Membrane Extended, 30mm x 40mm, Reference Number 5303-342 - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets; localized ridge augmentation for later implantation; alveolar ridge reconstruction for prosthetic treatment; filling of bone defects; guided bone regeneration in dehiscence defects and guided tissue regeneration procedures in periodontal defects.

Z-0912-2020
Recall number
Z-0912-2020
Initiated
November 05, 2019
Classification
Class II
Status
Terminated
Recalling firm
Collagen Matrix Inc
Quantity
192 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products may have been packaged with an incorrect Instructions for Use.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The products may have been packaged with an incorrect Instructions for Use.

Code information

UDI: (01)00366975013293(17)200630; Lot Number EPDMU18H1

Distribution pattern

US Nationwide distribution in the states of AR, AZ, CA, CO, FL, IL, MA, MD, MI, MN, NC, NJ, NY, OK, PA, SC, TX, UT, VA, and WA.