PriMatrix Fenestrated; Dermal Repair Scaffold; Rx Only; Sizes 4x4 cm, 6x6 cm, 8x8 cm, 14mm Disc, 18mm Disc, 2x2 cm, and 10x25 cm (Meshed 2:1).
Reported: July 12, 2023 Initiated: May 23, 2023 #Z-2078-2023
Product Description
PriMatrix Fenestrated; Dermal Repair Scaffold; Rx Only; Sizes 4x4 cm, 6x6 cm, 8x8 cm, 14mm Disc, 18mm Disc, 2x2 cm, and 10x25 cm (Meshed 2:1).
Reason for Recall
Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.
Details
- Recalling Firm
- TEI Biosciences, Inc.
- Units Affected
- 30,528 units
- Distribution
- Domestic: Nationwide Distribution.
- Location
- Boston, MA
Frequently Asked Questions
What product was recalled? ▼
PriMatrix Fenestrated; Dermal Repair Scaffold; Rx Only; Sizes 4x4 cm, 6x6 cm, 8x8 cm, 14mm Disc, 18mm Disc, 2x2 cm, and 10x25 cm (Meshed 2:1).. Recalled by TEI Biosciences, Inc.. Units affected: 30,528 units.
Why was this product recalled? ▼
Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 12, 2023. Severity: Moderate. Recall number: Z-2078-2023.
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