Neotract Inc recalls UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool
There is the potential that during implant deployment, the device may not properly deliver a implant.
Read the official notice →- Date
- 2022-08-10
- Country
- United States
- Brand
- Neotract Inc
- Product
- UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool
- Classification
- Class II
- Units
- US: AK AL AR AZ CA CO CT DC DE FL GA IA IL IN KS KY LA MA MD ME MI MN MO MS MT…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2022-08-17
USMckesson Medical-Surgical Inc. Corporate Office recalls Systane Zaditor, ketotifen fumarate ophthalmic solution 0.035%, Antihistamine eye drops, Eye Itch Relief, up to…
CGMP Deviations: products were stored outside the drug label specifications.
- US
Hikma Pharmaceuticals USA Inc. recalls Ativan Injection (lorazepam injection, USP), 2mg/mL, 1 mL vial, 25 vials per carton, RX Only, Manufactured by West-Ward…
Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.
- US
Glenmark Pharmaceuticals Inc., USA recalls Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/25 mg, 30 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals…
Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .
- 2022-08-10
- US
Turbett Surgical, Inc. recalls Turbett Surgical Container, TS1500
Devices were subject to unapproved rework processes.
- US
Craftmatic Industries, Inc. recalls Craftmatic Model 1 Base for Dual Bed Configurations
A potential for dual-configured beds to separate or slip away from one another.
FDA · DeviceCraftmatic Industries, Inc.US Nationwide distribution - product was not distributed outside of the United…Official notice → - US
Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Iron_2 (Iron_2) is for in vitro diagnostic use in the quantitative determination of iron in human serum and…
Falsely Elevated Atellica CH Microalbumin_2 (¿ALB_2) Results due to Reagent Carryover from the Iron_2 Assay. This defect occurs only when a microalbumin test is run immediately after an iron test.
FDA · DeviceSiemens Healthcare Diagnostics, Inc.Worldwide distribution - US Nationwide and the countries of AR, AU, AT, BS,…Official notice →