Drugs & medicalClass II

Turbett Surgical, Inc. recalls Turbett Surgical Container, TS1500

Devices were subject to unapproved rework processes.

Read the official notice →
Date
2022-08-10
Country
United States
Brand
Turbett Surgical
Product
Turbett Surgical Container, TS1500
Classification
Class II
Units
US Nationwide Nationwide: CO, FL, NC 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 Details may be shortened or out of date; the official notice is the authoritative source.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

  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.

More Turbett Surgical recalls

  1. 2023-02-08
  2. US
    Drugs & medicalClass II

    Turbett Surgical, Inc. recalls Turbett Surgical Container, TS1000: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider

    Pod may have weld failures breaching the sterile barrier and result in the use of unsterile instruments leading to infection or other major injuries.

    FDA · DeviceTurbett Surgical, Inc.US Nationwide distribution in the states of CA, IA, IN, NC, NH, NY, OH, LA,…Official notice →
  3. 2022-05-25
  4. US
    Drugs & medicalClass II

    TURBETT SURGICAL, LLC recalls Turbett Surgical Container, TS1500

    Eight units manufactured before June 2019 have exhibited weld failures breaching the sterile barrier after prolonged use.

    FDA · DeviceTURBETT SURGICAL, LLCDomestic distribution to PA, CA, and NY only.Official notice →
All 3 Turbett Surgical recalls →

Other drugs & medical recalls in the United States

  1. 2022-08-17
  2. US
    Drugs & medicalClass II

    Hikma Pharmaceuticals USA Inc. recalls Ativan Injection (lorazepam injection, USP), 2mg/mL, 1 mL vial, 25 vials per carton, RX Only, Manufactured by West-Ward…

    Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.

    FDA · DrugHikma Pharmaceuticals USA Inc.Nationwide in the USAOfficial notice →
  3. US
    Drugs & medicalClass II

    Glenmark Pharmaceuticals Inc., USA recalls Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/25 mg, 30 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals…

    Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .

    FDA · DrugGlenmark Pharmaceuticals Inc., USAnationwideOfficial notice →
  4. 2022-08-10
  5. US
    Drugs & medicalClass II

    Neotract Inc recalls UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool

    There is the potential that during implant deployment, the device may not properly deliver a implant.

    FDA · DeviceNeotract IncUS: AK AL AR AZ CA CO CT DC DE FL GA IA IL IN KS KY LA MA MD ME MI MN MO MS MT…Official notice →
  6. US
    Drugs & medicalClass II

    Craftmatic Industries, Inc. recalls Craftmatic Model 1 Base for Dual Bed Configurations

    A potential for dual-configured beds to separate or slip away from one another.

    FDA · DeviceCraftmatic Industries, Inc.US Nationwide distribution - product was not distributed outside of the United…Official notice →
  7. US
    Drugs & medicalClass II

    Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Iron_2 (Iron_2) is for in vitro diagnostic use in the quantitative determination of iron in human serum and…

    Falsely Elevated Atellica CH Microalbumin_2 (¿ALB_2) Results due to Reagent Carryover from the Iron_2 Assay. This defect occurs only when a microalbumin test is run immediately after an iron test.

    FDA · DeviceSiemens Healthcare Diagnostics, Inc.Worldwide distribution - US Nationwide and the countries of AR, AU, AT, BS,…Official notice →
  8. US
    Drugs & medicalClass II

    St. Jude Medical, Cardiac Rhythm Management Division recalls Merlin 2 PCS MER37000 programmer Model MER3400 software

    The Merlin" 2 PCS model MER3700 is a portable, dedicated programming system designed to interrogate, program, display data from, and test Abbott Medical implantable medical devices during implant and follow-up.

    FDA · DeviceSt. Jude Medical, Cardiac Rhythm Management DivisionUS: AK AL AR AZ CA CO CT DC DE FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO…Official notice →
See all drugs & medical recalls →