Recall Atlas
Drugs & medicalClass II

ORTHOPEDIATRICS CANADA ULC Dba PEGA MEDICAL recalls FRT250 - 4.0-6.4 CARTRIDGE. Component of the Fassier-Duval Telescopic IM System

During the assembly of the FRT250 cartridge assembly, an incorrect component was used. Specifically, the FRT240-HEX (2) was used instead of the FRT250-HEX.

Read the official notice →
Date
2024-09-04
Country
United States
Brand
ORTHOPEDIATRICS CANADA ULC Dba PEGA MEDICAL
Product
FRT250 - 4.0-6.4 CARTRIDGE. Component of the Fassier-Duval Telescopic IM System
Classification
Class II
Units
Worldwide - US Nationwide distribution in the state of Texas and the countries…
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 Details may be shortened or out of date; the official notice is the authoritative source.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

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. 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.

Other drugs & medical recalls in the United States

  1. 2024-09-11
  2. US
    Drugs & medicalClass II

    Beckman Coulter, Inc. recalls DxI 9000 Access Immunoassay Analyzer, REF C11137, vitro diagnostic device used for the quantitative, semi-quantitative, or qualitative…

    Beckman Coulter manufacturing discovered cracks around a threaded insert on the bottom of the Internal Wash Buffer Tank that is used within the Wash Buffer Supply Drawer on the DxI 9000.This can result in leaking,…

    FDA · DeviceBeckman Coulter, Inc.Worldwide - US Nationwide distribution in the state of New Hampshire and the…Official notice →
  3. US
    Drugs & medicalClass II

    ProRx LLC recalls Tirzepatide 2 mL (10 mg/mL) and 20 mg/mL, 2mL Multidose SC Injection vials, Compounded Rx Product, ProRx 267-565-7008, NDC 84139-210-01

    Lack of Assurance of Sterility

    FDA · DrugProRx LLCNationwide in the USAOfficial notice →
  4. US
    Drugs & medicalClass I

    Baxter Healthcare Corporation recalls Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection), 2,000 units per 1,000 mL (2 units/mL), 1000 mL Sterile Single Dose…

    Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.

    FDA · DrugBaxter Healthcare CorporationNationwide in the USAOfficial notice →
  5. 2024-09-04
  6. US
    Drugs & medicalClass II

    Cypress Medical Products LLC recalls McKesson Syringe 60CC, Luer Lock Tip, Sterile, ITEM NO 102-S60C. Model No. 102-S60C - SYRINGE, LL 60CC (25/BX 4BX/CS)

    Affected syringes lack FDA clearance.

    FDA · DeviceCypress Medical Products LLCUS distribution only. Domestic distribution nationwide.Official notice →
  7. US
    Drugs & medicalClass II

    Beaver Visitec International, Inc. recalls BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001113;

    Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in some of BVI CustomEyes Procedure…

    FDA · DeviceBeaver Visitec International, Inc.US Nationwide distribution.Official notice →
  8. US
    Drugs & medicalClass II

    Beaver Visitec International, Inc. recalls BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584550;

    Data in RES.

    FDA · DeviceBeaver Visitec International, Inc.US Nationwide distribution.Official notice →
See all drugs & medical recalls →