Stryker Corporation recalls Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube Sets are intended to be used with the…
Due to nonconforming products being inadvertently distributed.
Read the official notice →- Date
- 2026-05-20
- Country
- United States
- Brand
- Stryker
- Product
- Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube Sets are intended to be used with the…
- Classification
- Class II
- Units
- U.S. Nationwide distribution in the state of GA.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Stryker recalls
- 2026-08-12
USStryker Corporation recalls STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0250070640
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
FDA · DeviceStryker CorporationWorldwide distribution - US Nationwide and the countries of Australia, Brazil,…Official notice →- 2026-08-05
- US
Stryker GmbH recalls Stryker Hoffmann II Connecting Rod Micro 3 x 40mm. Catalog Number: 50796040.
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
FDA · DeviceStryker GmbHWorldwide - US Nationwide distribution including in the states of AL, AZ, CA,…Official notice → - 2026-06-10
- US
Stryker Corporation recalls Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being shipped to your facility. There is a…
- 2026-02-25
- US
Stryker Corporation recalls MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN): 00850024195028 MS-00009…
Due to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target tissue removal procedures.
FDA · DeviceStryker CorporationWorldwide - U.S. Nationwide distribution including in the states of AL, AK,…Official notice → - 2025-12-03
- US
Stryker Corporation recalls NICO BrainPath; Product Number/Product Name NN-8024 BrainPath Shephard's Hook - Greenberg; NN-8025 BrainPath Shephard's Hook - Sugita;…
Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.
FDA · DeviceStryker CorporationWorldwide distribution - US Nationwide and the countries of Australia,…Official notice → - 2025-08-13
- US
Stryker Corporation recalls Stryker SmartPump Tourniquet, disposable sterile (single use) DISP 18X3,1BLA,1PRT QUICK / 5921-018-135; DISP 18X3,1BLA,2PRT QUICK /…
Tourniquet cuff flange may become detached from the bladder. If leak occurs during the procedure, there may be risk of hemorrhage, resulting in blood loss greater than expected. Other serious risks include cerebral…
FDA · DeviceStryker CorporationDomestic US distribution nationwide. International distribution to Australia…Official notice →
Other drugs & medical recalls in the United States
- 2026-05-20
- US
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion. System Code Description (Model Number): Azurion 3 M12 (722221, 722229), Azurion 3 M15 (722222, 722230),…
Potential for the bolts and plastic parts of the Cable Hose Carriers that hold the cable hose to the monitor ceiling suspension may loosen and/or break over time due to the forces applied when the monitor is moved or…
FDA · DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Worldwide distribution - US Nationwide and the country of Canada.Official notice → - US
Quidel Corporation recalls QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.
Product has the potential for false positive results
FDA · DeviceQuidel CorporationUS Nationwide distribution in the states of AL, CA, FL, ID, IL, LA, MA, MD,…Official notice → - US
Hologic, Inc recalls SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers: SDA-SYS-3000-2D-HTC, SDA-SYS-3000-3D, SDM-SYS-6000-2D, SDM-SYS-6000-3D,…
Complaints have been received of systems developing loose, missing, or broken internal bolts over time.
- US
Dexcom, Inc. recalls Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM watchOS App Model/Catalog Number: SW13355 Software…
A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows. When the app is running in the background, EGV…
FDA · DeviceDexcom, Inc.SW12300 & SW13355 Dexcom G7 iOS and watchOS app versions 2.9.0 through 2.11.2:…Official notice → - US
Technological Medical Advancements LLC recalls Diowave Laser System, REF: Diowave 250W
Software update is needed for laser systems, for topical infrared heating to provide temporary relief of minor muscle and joint pain, spasms, stiffness associated with minor arthritis, and to temporarily increase local…
FDA · DeviceTechnological Medical Advancements LLCUS Nationwide distribution in the states of TX, CA, MI, MD, PA, FL, MN, DC, MI.Official notice → - US
Jolife AB recalls LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model Number: 99576 Catalog…
Due to a subset of chest compression systems/devices where the service performed on the systems were not appropriately documented (The documents for the service performed to justify the passing results were not include…
FDA · DeviceJolife ABU.S. Nationwide distribution in the states of AL, AZ, CA, FL, HI, IA, KS, KY,…Official notice →