Collagen Matrix Inc

Complete recall history across all FDA and CPSC categories — 11 total recalls

Collagen Matrix Inc appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (11)

FDA medical device enforcement actions by Collagen Matrix Inc

Date Product Reason Class
Aug 3, 2022 Collagen Dental Wound Dressing - Bovine Dermis Tap, 25mm x 75mm Product wa... The packaging may not be sealed, which could compromise sterility. Class II
Nov 5, 2019 GIBSON Healthcare Membrane Extended, 30mm x 40mm, Reference Number 5303-342 -... The products may have been packaged with an incorrect Instructions for Use. Class II
Nov 5, 2019 GIBSON Healthcare Membrane 6-9, 20mm x 30mm, Reference Number 5303-235 - Prod... The products may have been packaged with an incorrect Instructions for Use. Class II
Nov 5, 2019 GIBSON Healthcare Membrane 6-9, 30mm x 40mm, Reference Number 5303-299 - Prod... The products may have been packaged with an incorrect Instructions for Use. Class II
Nov 5, 2019 GIBSON Healthcare Membrane 6-9, 15mm x 20mm, Reference Number 5303-226 - Prod... The products may have been packaged with an incorrect Instructions for Use. Class II
Nov 5, 2019 GIBSON Healthcare Membrane Extended, 15mm x 20mm, Reference Number 5303-306 -... The products may have been packaged with an incorrect Instructions for Use. Class II
Nov 5, 2019 GIBSON Healthcare Membrane Extended, 20mm x 30mm, Reference Number 5303-324 -... The products may have been packaged with an incorrect Instructions for Use. Class II
Oct 30, 2018 Porcine Anorganic Bone Mineral 4.0cc There is a possibility that the product labeled as 4.0cc volume may only con... Class III
Nov 17, 2015 ZCORE Porcine Xenograft Particulate in Syringe Product Intended for use in... The distributor, Osteogenics Biomedical, notified the firm that the syringes... Class III
Aug 25, 2015 NuOSS Cancellous Intended for use in dental surgery. On 8/25/2015, Collagen Matrix, Inc discovered that one of the 171 units of Nu... Class II
May 13, 2013 NuOss XC Sinus Reference No 509-3001 (BMCU17, size 17 mm diameter x 10 mm he... During the 36 month real time shelf life testing of NuOss XC Sinus (BMCU-Umbr... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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