Drugs & medicalClass II

Stradis Healthcare recalls Surgical Suture Kit

There is uncertainty about the integrity of the methods used to ensure the sterile barrier integrity.

Read the official notice →
Date
2022-06-01
Country
United States
Brand
Stradis Healthcare
Product
Surgical Suture Kit
Classification
Class II
Units
US Distribution to NC.
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Stradis Healthcare recalls

  1. 2023-01-18
  2. US
    Drugs & medicalClass II

    Stradis Healthcare recalls McCormick Medical Distribution PORT TRAY, 25 trays per case. Distributed by McCormick Medical Distribution.

    Potential for the outer bag having pinhole leaks near the seal, which may result in a breach in the sterility of the kit.

    FDA · DeviceStradis HealthcareUS Nationwide distribution in the states of FL, IL, IN, MA, MS, NV, OH, TN,…Official notice →
  3. 2022-09-14
  4. US
    Drugs & medicalClass II

    Stradis Healthcare recalls VYGON DRESSING CHANGE W/MAXISWAB kit, REF AMS-8465CS

    Potential for incomplete seals.

    FDA · DeviceStradis HealthcarePennsylvaniaOfficial notice →
All 3 Stradis Healthcare recalls →

Other drugs & medical recalls in the United States

  1. 2022-06-01
  2. US
    Drugs & medicalClass II

    Umano Medical, Inc. recalls AC-powered adjustable medical beds with built-in electric DC actuators and controls.

    There is a potential hazard of uninterrupted motion of the Motorized Wheel System due to the possible failure of a component in the electrical system of the Product.

    FDA · DeviceUmano Medical, Inc.Worldwide distribution - US Nationwide distribution in the states of CA, PA,…Official notice →
  3. US
    Drugs & medicalClass II

    ConvaTec, Inc recalls SUR-FIT Natura S4S Durahesive Wafer 70MM (1X10PK) US. Each market unit contains 10 individual wafers.

    Firm received 10 complaints of skin barrier delamination issues (e.g. flange lifts from wafer, skin barrier layers separate) or tape border rips/tears.

    FDA · DeviceConvaTec, IncDistributed nationwide to NJ, PA, OH, CA, AL, MI, NY, TX, FL, NC, VA, LA, IL,…Official notice →
  4. US
    Drugs & medicalClass II

    Smith & Nephew Orthopaedics GmbH recalls INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right

    Right nails were anodized, marked, and labelled as left nails and vice versa

    FDA · DeviceSmith & Nephew Orthopaedics GmbHDistributed nationwide to GA, OH, IN, TX, CO, MO, TN, CA, NC, PA and…Official notice →
  5. US
    Drugs & medicalClass II

    Medtronic Perfusion Systems recalls Cardioblate" Gemini"-s Irrigated RF Surgical Ablation System; The device is placed in a plastic tray with a snap on plastic lid, the…

    Firm detected an increase in complaints related to fractured jaw tips of the Cardioblate Gemini-s.

    FDA · DeviceMedtronic Perfusion SystemsWorldwide distribution - US Nationwide distribution in the states of CA, ND,…Official notice →
  6. US
    Drugs & medicalClass II

    Invacare Corporation recalls Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V

    The battery wiring harness on affected wheelchairs may become disconnected during shipment from the factory or during wheelchair use traversing large obstacles or after a jolt or impact to the wheelchair. The…

    FDA · DeviceInvacare CorporationWorldwide distribution - US Nationwide distribution in the states of AK, AR,…Official notice →
  7. US
    Drugs & medicalClass II

    Medtronic Neuromodulation recalls Percept PC BrainSense Implantable Neurostimulator (INS) Model B35200

    The Implantable Neurostimulator (INS) cannot communicate with the clinical programmer and/or the patient programmer system.

    FDA · DeviceMedtronic NeuromodulationWorldwide distribution - US Nationwide distribution in the states of AK, AL,…Official notice →
See all drugs & medical recalls →