Preat Corp recalls Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
Due to a manufacturing issue, the screw seat location on the abutment product may be too high, causing mating screw to have a shorter engagement length into the associated implant.
Read the official notice →- Date
- 2024-03-27
- Country
- United States
- Brand
- Preat
- Product
- Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
- Classification
- Class II
- Units
- U.S. Nationwide distribution in the states of AZ, OH and PA.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Preat recalls
- 2025-06-25
USPreat Corp recalls Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with…
Due to manufacturing issues, abutment products were manufactured with screw seat located too high, which may cause the mating screw to have a shorter engagement length into the associated implant.
FDA · DevicePreat CorpU.S. Nationwide distribution in the states of AZ, CA, GA, MO, NJ, NY, OH, PA,…Official notice →- 2024-08-28
- US
Preat Corp recalls Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible 6.0mm Digital Analog, REF 9000703 Straumann…
Due to a manufacturing issue, the product has a out of specification rotation of the digital analog used to visually inspect dental abutments and restorations.
FDA · DevicePreat CorpU.S. Nationwide distribution in the states of AK, AZ, FL, GA, IL, LA, MD, MI,…Official notice → - 2024-07-17
- US
Preat Corp recalls 9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixture…
Due to incorrect milled titanium abutment being packaged and labeled.
- 2023-11-01
- US
Preat Corp recalls Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental
The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage
- 2023-04-05
- US
Preat Corp recalls Neodent GM X 6mm Engaging Titanium Base, REF: 9007162
Engaging titanium base contains a dimensional condition that allows vertical movement of the titanium base after the prosthetic screw is torqued to the recommended value, which if undetected and installed on the…
- 2023-03-15
- US
Preat Corp recalls PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic glue.
Product is labeled with an incorrect expiration date.
FDA · DevicePreat CorpWorldwide - US Nationwide distribution including in the states of AL, AZ, CA,…Official notice →
Other drugs & medical recalls in the United States
- 2024-03-27
- US
Baxter Healthcare Corporation recalls HDS Traction Boot II, REF AR-6529-23, The Traction Boot is designed to position, support and/or distract the patient's foot for…
Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Hip Distraction System, Traction Boot II, due to the boots being assembled incorrectly. The locking ridge on the front face of the boot…
FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution in the state of Florida.Official notice → - US
Randox Laboratories Ltd. recalls Liquid Protein Calibrators. C3 and Haptoglobin liquid protein calibrators used with Randox IgA, IgG, and IgM assays that require sample…
The firm has realigned C3 and Haptoglobin in Liquid Protein Calibrators, IT2691, to reference material ERM-DA470k/IFCC.
- US
Thommen Medical AG recalls impression coping, repositionable, short, screw-retained, PF 4.0
The depth of the internal canal was not manufactured according to specifications. Thus, the impression coping cannot be firmly connected to the implant.
FDA · DeviceThommen Medical AGUS Nationwide distribution in the states of OH and KY.Official notice → - US
In2Bones, SAS recalls I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 80mm,Part Number S65 ST180
This Field Action is being conducted following the identification of a batch mix-up between I.B.S Compression screws diameter 6.5mm length 75mm and I.B.S Compression screws diameter 6.5mm length 80mm. The screws of the…
- US
Think Surgical, Inc. recalls Assembly, Array Guide TMINI, REF: 109101, part of the TMINI Knee Instrument Set, used with the TMINI Miniature Robotic System
There is a galling effect (cold-weld) caused by friction between the array fixation pins and the TMINI array guide holes due to insufficient clearance between the outer diameter of the fixation pins and the inner…
FDA · DeviceThink Surgical, Inc.US Nationwide distribution in the states of AL, OH, NV, TX, UT, CA, MO.Official notice → - US
Medtronic Inc. recalls Abre Venous Self-expanding Stent System, Product Numbers: a) AB9U14080090; b) AB9U18100090; c) AB9G14100090
There is a potential for sterile package breach.
FDA · DeviceMedtronic Inc.Worldwide distribution - US Nationwide and the countries of Australia, Canary…Official notice →