D.O.R.C. Dutch Opthalmic Research Center Intl B.V. recalls TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02,…
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
Read the official notice →- Date
- 2026-06-17
- Country
- United States
- Brand
- D.O.R.C. Dutch Opthalmic Research Center Intl
- Product
- TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02,…
- Classification
- Class II
- Units
- Worldwide - US Nationwide and the countries of AUSTRALIA, AUSTRIA, BELGIUM,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- 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 D.O.R.C. Dutch Opthalmic Research Center Intl recalls
- 2024-03-27
USD.O.R.C. Dutch Opthalmic Research Center Intl B.V. recalls Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)
When using those products you may experience difficulties to extend or retract the laser fiber, and in some occasions may also have difficulties to direct the laser fiber tip precisely.
FDA · DeviceD.O.R.C. Dutch Opthalmic Research Center Intl B.V.US Nationwide distribution in the states of AZ, CO, FL, IN, MD, NC, NY, OH,…Official notice →
Other drugs & medical recalls in the United States
- 2026-06-17
- US
Avanos Medical, Inc. recalls Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- US
HF Acquisition Co LLC recalls Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS…
Due to incorrect incubation process being performed on product.
FDA · DeviceHF Acquisition Co LLCU.S. Nationwide distribution including in the states of AR, AZ, CA, CO, CT,…Official notice → - US
INSPIREMD Inc recalls Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: CND0840
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
FDA · DeviceINSPIREMD IncUS Nationwide distribution in the states of AR, AZ, CA, DC, FL, GA, HI, IL,…Official notice → - US
Fresenius Medical Care Holdings, Inc. recalls Bicarby" Dialysate; Model Numbers: RFP-400-G, RFP-401-G, RFP-402-G, RFP-404-G, RFP-407-G, and RFP-456-G;
Given the increased number of leaks reported by users, it was determined to be the appropriate course of action to notify users of the potential for the occurrence of Bicarby luer-lock leaks during manipulation of the…
FDA · DeviceFresenius Medical Care Holdings, Inc.US Nationwide distribution in the states of NY, TN and TX.Official notice → - US
BERLIN HEART GMBH recalls EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves: 10 ml, REF: P10P-001; 30 ml, REF: P30P-001x01
Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.
- US
Mozarc Medical US LLC recalls Mahurkar Elite PASS Trays; Description (Product Number/CFN): 12 FR x 13cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray…
The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays.