Drugs & medicalClass II

Davol, Inc. recalls Ventralight ST w Echo PS 4.5" Circle A low profile, bioresorbable, coated, permanent mesh, with a pre-attached removable positioning…

Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequate mesh placement, erosion/migration,…

Read the official notice →
Date
2023-08-02
Country
United States
Brand
Davol
Product
Ventralight ST w Echo PS 4.5" Circle A low profile, bioresorbable, coated, permanent mesh, with a pre-attached removable positioning…
Classification
Class II
Units
Worldwide distribution - US Nationwide and the countries of Belgium, Czech…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Davol recalls

  1. 2026-04-29
  2. US
    Drugs & medicalClass II

    Davol, Inc. recalls Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm. Catalog Number: 1050030.

    Potential for product to contain foreign matter, confirmed to be inspect fragments.

    FDA · DeviceDavol, Inc.Worldwide distribution - US Nationwide and the countries of China, South Korea.Official notice →
  3. 2022-08-03
  4. US
    Drugs & medicalClass II

    Davol, Inc. recalls X-Stream Irrigation System (Catalog No. 5551000) and X-Stream Irrigation System Refurbished (Catalog No. 9551000)

    The device may potentially cause a fire, leading to a safety risk.

    FDA · DeviceDavol, Inc.Worldwide distribution - US Nationwide and the countries of Canada and Chile.Official notice →
  5. 2022-07-06
  6. US
    Drugs & medicalClass II

    Davol, Inc. recalls HydroSurg Plus Laparoscopic Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, 33cm Tip and Cojoined Suction and Irrigation Tubing,…

    The product is not able to provide irrigation.

    FDA · DeviceDavol, Inc.Worldwide distribution - US Nationwide and the country of Canada.Official notice →
All 4 Davol recalls →

Other drugs & medical recalls in the United States

  1. 2023-08-09
  2. US
    Drugs & medicalClass II

    Central Admixture Pharmacy Services, Inc. recalls Neonatal TPN Starter Bag, Amino Acids (trophamine) 3%/Dextrose 5% with CALCIUM, total volume = 250mL, IV Bag, Rx Only,…

    Lack of assurance of sterility. Validation data for decontamination cycles is lacking.

    FDA · DrugCentral Admixture Pharmacy Services, Inc.Nationwide in the USAOfficial notice →
  3. US
    Drugs & medicalClass II

    The Ritedose Corporation recalls Cromolyn Sodium Oral Solution (Concentrate) 100 mg/5 mL 96 Plastic Ampules per carton, Rx Only, For Oral Use Only - Not For Inhalation…

    CGMP deviation: product released prior to supplier approval.

    FDA · DrugThe Ritedose CorporationNationwide in the USOfficial notice →
  4. 2023-08-02
  5. US
    Drugs & medicalClass II

    Qiagen GmbH recalls QIAstat-Dx Respiratory SARS-CoV-2 Panel -US IVD qualitative test intended for analyzing nasopharyngeal swab (NPS) samples from patients…

    Identified a decreased performance reliability rate, Run abortions could cause delayed diagnosis since sample testing would have to be repeated

    FDA · DeviceQiagen GmbHDC, AL, CA, FL, GA, ME, NC, NY, OR, TX Foreign: DE, AE, AT, BE, BG, CH, CL,…Official notice →
  6. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls Cios Select VA 21 with FD- A Mobile X-ray system intended for use in Operating room, Traumatology, Endoscopy, Intensive Care…

    Incorrect glue was applied on the plexiglass sheet on the single tank cover assembly could potentially fall off and the ingress of liquid may occur, the risk of electric shock exists (e.g., ingress of a large amount of…

    FDA · DeviceSiemens Medical Solutions USA, IncWorldwide - US Nationwide distribution in the states of FL, GA, KS, MN, NC, NY…Official notice →
  7. US
    Drugs & medicalClass II

    Argon Medical Devices, Inc recalls Argon Medical Devices, REF 352506070E, Option Elite Retrievable Vena Cava Filter, Suitable of Jugular or Femoral Delivery, STERILEO,…

    There is the potential that the vena Cava Filter may not perform as intended which may result in pulmonary embolism.

    FDA · DeviceArgon Medical Devices, IncUS Nationwide distribution in the state of TX.Official notice →
  8. US
    Drugs & medicalClass II

    MICROVENTION INC. recalls FRED Flow Re-Direction Endoluminal Device, REF: FRED3507-PMA, FRED3511, FRED3511-PMA, FRED3516-CA, FRED3516-PMA, FRED3524, FRED3524-CA,…

    Intracranial aneurysm flow diverter device may be manufactured with an incorrect inner stent length and may not perform as intended.

    FDA · DeviceMICROVENTION INC.Worldwide - US Nationwide distribution including in the states of AZ, NY, FL,…Official notice →
See all drugs & medical recalls →