Preat Corp
Complete recall history across all FDA and CPSC categories — 11 total recalls
Preat Corp 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 Preat Corp
| Date | Product | Reason | Class |
|---|---|---|---|
| Jun 25, 2025 | NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base, REF: 9000662 | Engaging titanium base was manufactured 180 degrees around the post from wher... | Class II |
| Jun 24, 2025 | Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 90... | Due to manufacturing error, digital analog rotational feature is 180 degrees ... | Class II |
| Apr 2, 2025 | Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat... | Due to manufacturing issues, abutment products were manufactured with screw s... | Class II |
| Jun 25, 2024 | Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatibl... | Due to a manufacturing issue, the product has a out of specification rotation... | Class II |
| Apr 10, 2024 | 9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too b... | Due to incorrect milled titanium abutment being packaged and labeled. | Class II |
| Feb 9, 2024 | Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967 | Due to a manufacturing issue, the screw seat location on the abutment product... | Class II |
| Jul 18, 2023 | Preat REF 9007123, Neodent GM x 4mm Healing Abutment, Rx Only, Non-Sterile, S... | The healing abutments contain a dimensional condition that may lead to a gap ... | Class II |
| Jul 18, 2023 | Preat REF 9007124, Neodent GM x 4mm Healing Abutment (Wide), Rx Only, Non-Ste... | The healing abutments contain a dimensional condition that may lead to a gap ... | Class II |
| Jul 18, 2023 | Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, S... | The healing abutments contain a dimensional condition that may lead to a gap ... | Class II |
| Feb 21, 2023 | Neodent GM X 6mm Engaging Titanium Base, REF: 9007162 | Engaging titanium base contains a dimensional condition that allows vertical ... | Class II |
| Feb 1, 2023 | PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials... | Product is labeled with an incorrect expiration date. | Class III |
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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