Drugs & medicalClass II

Applied Medical Resources Corp recalls Epix Universal Clip Applier, REF: CA500, STERILEEO

Their is the potential that Universal Clip applier may not load clip after the trigger is actuated.

Read the official notice →
Date
2024-04-03
Country
United States
Brand
Applied Medical Resources
Product
Epix Universal Clip Applier, REF: CA500, STERILEEO
Classification
Class II
Units
Worldwide - US Nationwide distribution including in the states of AK, AL, AR,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Applied Medical Resources recalls

  1. 2026-01-14
  2. US
    Drugs & medicalClass II

    Applied Medical Resources Corp recalls Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23

    There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.

    FDA · DeviceApplied Medical Resources CorpUS: MI, CA, ME, OUS: France Great Britain, GermanyOfficial notice →
All 2 Applied Medical Resources recalls →

Other drugs & medical recalls in the United States

  1. 2024-04-03
  2. US
    Drugs & medicalClass II

    Medical Action Industries, Inc. 306 recalls IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.

    The kits contain saline flush syringes which were recalled by the supplier.

    FDA · DeviceMedical Action Industries, Inc. 306US Nationwide distribution in the states of MN and ND. There as no…Official notice →
  3. US
    Drugs & medicalClass II

    Puritan Medical Products Company, Llc recalls HydroFlock Sterile Flocked Collection Device, Part Number 25-3317-H.

    It was discovered through a customer complaint that mislabeled product was distributed. Puritan distributed product labelled as 25-3317-H lot S1014 which contained product code 25-3317-U in all packages.

    FDA · DevicePuritan Medical Products Company, LlcWorldwide - US Nationwide distribution in the states of AL, CA, FL, GA, IA,…Official notice →
  4. US
    Drugs & medicalClass II

    Boston Scientific Corporation recalls Boston Scientific iSLEEVE EXPANDABLE Introducer Set REF H74939349140, facilitates femoral access to the vascular system

    Boston Scientific is conducting a removal of specific batches of the iSLEEVETM 14F Expandable Introducer Set due to complaints associated with a hemostatic valve leak.

    FDA · DeviceBoston Scientific CorporationWorldwide distribution - US Nationwide and the countries of Canada.Official notice →
  5. US
    Drugs & medicalClass II

    Philips North America recalls CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Version Number C.03.X

    It was found that the Care Assist mobile application (version 4.1.1 and earlier) would not play custom ringtones when iOS device screens were locked with a passcode.

    FDA · DevicePhilips North AmericaWorldwide - US Nationwide distribution.Official notice →
  6. US
    Drugs & medicalClass II

    Olympus Corporation of the Americas recalls SOLTIVE Pro SuperPulsed Laser (TFL-SLS )

    A non-compliant power cord may have been supplied in regions that do not utilize the Type B or Type E/F plug configurations.

    FDA · DeviceOlympus Corporation of the AmericasDomestic: OUS Only; International distribution in the states of Australia,…Official notice →
  7. US
    Drugs & medicalClass II

    Bolton Medical Inc. recalls RELAY PRO Thoracic Stent-Graft System, containing one endovascular stent-graft system, IFU, and patient tracking card, sterile: (a) Part…

    The stent-graft inside the delivery system was the incorrect size.

    FDA · DeviceBolton Medical Inc.Worldwide - US Nationwide distribution in the states of AZ, MA, and TX. The…Official notice →
See all drugs & medical recalls →