Recall Register

Food, drugs, devices › Firms

Preat Corp

FDA recalling firm · 9 enforcement events · 11 product records · 2023–2025 · CA

Preat Corp has 9 FDA enforcement events on this register (11 product records) between 2023 and 2025: 9 device; the busiest year was 2023 with 3.

0% of its events are Class I; the most common class is Class II (8). 9 events are listed as ongoing; the recalling firm's address is in CA.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
25 Jun 2025NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base, REF: 9000662DeviceClass II1Ongoing
24 Jun 2025Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx OnlyDeviceClass II1Ongoing
2 Apr 2025Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch to provide support for single-unit or multi-unit prosthetic restorations.DeviceClass II1Ongoing
25 Jun 2024Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible 6.0mm Digital Analog, REF 9000703 Straumann Tissue-Level-compatible WN Digital Analog, REF 9001303 3i Certain-compatible 5.0mm Digital Analog, REF 9001903 3i Certain-compatible 6.0mm Digital Analog, REF 9002003 Astra-compatible 3.0mm…DeviceClass II1Ongoing
10 Apr 20249006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixture to aid in prosthetic rehabilitation.DeviceClass II1Ongoing
9 Feb 2024Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967DeviceClass II1Ongoing
18 Jul 2023Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. DentalDeviceClass II3Ongoing
21 Feb 2023Neodent GM X 6mm Engaging Titanium Base, REF: 9007162DeviceClass II1Ongoing
1 Feb 2023PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic glue.DeviceClass III1Ongoing

By type and class

Device9
Class II8
Class III1

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

23
24
25
26
Enforcement events for Preat Corp by year initiated.

Questions and answers

How many FDA recalls has Preat Corp had?

9 enforcement events (11 product records) on this register, 2023–2025: 9 device.

Are any Preat Corp recalls ongoing?

9 events are listed as ongoing in the current openFDA export.

What class are Preat Corp recalls?

8 Class II, 1 Class III. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.