Retractable Technologies, Inc. recalls EasyPoint Needle, 25G x 5/8", REF: 82091
The needle cannula of a retractable needle may detach from the needle holder in the patient.
Read the official notice →- Date
- 2024-03-20
- Country
- United States
- Brand
- Retractable Technologies, Inc.
- Product
- EasyPoint Needle, 25G x 5/8", REF: 82091
- Classification
- Class II
- Units
- US Nationwide distribution including in the states of NY, FL, IL, MA, UT, NJ,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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.
Other drugs & medical recalls in the United States
- 2024-03-20
USWaldemar Link GmbH & Co. KG (Mfg Site) recalls SPII Model Lubinus, Long Stem Prosthesis XL Neck, cemented
Due to two complaints, has come to our attention that additional guidance is required on the correct interpretation of the carton label Size and Type columns to avoid misinterpretation during surgery.
FDA · DeviceWaldemar Link GmbH & Co. KG (Mfg Site)US Nationwide distribution in the states of AL, AZ, CA, FL, GA, ID, IL, IN,…Official notice →- US
MEDLINE INDUSTRIES, LP - Northfield recalls CVS Health Waterproof Wound Tracking Dressing, REF CVS690330, immediate package contains 1 sterile dressing, 4 in. x 4 in.,…
Product failed sterility testing.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the states of AL, CA, FL, IN, MI, MO, NJ, NY,…Official notice → - US
Beaver Visitec International, Inc. recalls BVI Visitec Irrigation Handle (20/SP)- Intended to be fit with a cannula for irrigation of the eye Catalog Number: 581012
Pack and pouch label is missing the manufacturing and expiration date.
FDA · DeviceBeaver Visitec International, Inc.Worldwide distribution - US Nationwide and the countries of AUSTRALIA, CANADA,…Official notice → - US
SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION recalls Shimadzu, Trinias, Digital Angiography System
Due to capacitor manufacturing issue, their is a potential that Flat Panel Device may have abnormal display or no function.
FDA · DeviceSHIMADZU CORPORATION MEDICAL SYSTEMS DIVISIONUS Nationwide distribution in the states of OH.Official notice → - US
Baxter Healthcare Corporation recalls CLEARLINK Non-DEHP Solution Set Luer Lock Adapter, Product Code 2R8401
Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Clearlink Non-DEHP solution set listed below due to potential leaks originating from the drip chamber.
- US
Biosense Webster, Inc. recalls CARTO VIZIGO Bi-Directional Guiding Sheath, REF D128502 The CARTO VIZIGOTM Bi-Directional Guiding Sheath is designed to provide…
Due to a manufacturing issue, device under process validation phase were inadvertently mixed into the main manufacturing process.
FDA · DeviceBiosense Webster, Inc.U.S. Nationwide distribution including in the states of FL, IL, AL, NY, PA,…Official notice →