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…
Read the official notice →- Date
- 2023-04-05
- Country
- United States
- Brand
- Preat
- Product
- Neodent GM X 6mm Engaging Titanium Base, REF: 9007162
- Classification
- Class II
- Units
- US Nationwide distribution in the states of TX, OR, UT, NY.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
US
Preat 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.
- 2024-03-27
US
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.
- 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
- 2023-03-15
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
- 2023-04-05
US
Alcon Research, LLC recalls Alcon Custom Pak Surgical Procedure Pack: Pak Number & Pak Description: 17533-04 DR GROSS LPS LLC 18704-03 CATARACT SURGI CARE 18382-03 DR…
Sterility; Steril surgical procedure packs contain incomplete seals.
FDA · DeviceAlcon Research, LLCUS: AL, AR, CA, IA, ID, IN, KY, MN, NC, ND, NJ, OH, PA, TX, OUS: NoneOfficial notice →US
GAGA PRO LIGHTING EQUIPMENT CO., recalls GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Light Show (LLS)projectors for the purposes of demonstration…
GAGA Pro LLS systems was not in compliance with the FDA's Performance Standard for laser products.
US
Randox Laboratories recalls CRP Immunoturbidimetric reagent. Intended for the quantitative in vitro determination of CRP concentration in serum Catalogue number: CP3826
The Antibody (R2 reagent) is showing a positive bias compared to previous batches on patient samples. Quality Controls do not show the same bias and will be within range
US
Ascend Laboratories, LLC recalls Dabigatran Etexilate 150mg Capsules, 150 mg, Rx Only, 60 Capsules per bottle, Manufactured by: Alkem Laboratories Ltd., INDIA,…
CGMP Deviations: Detection of N-nitroso-dabigatran (NDAB) impurity levels above the Acceptable Daily Intake Limit.
US
Apollo Care recalls Fentanyl 500mcg (2mcg/mL) and Ropivacaine HCl 250mg (1mg/mL) added to 250mL 0.9% Sodium Chloride, For Epidural Use Only, Rx only, 3801…
Lack of assurance of sterility: Suspected microbial growth present on external label packaging.
US