Sarnova HC, Llc recalls Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT
Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula.
Read the official notice →- Date
- 2026-10-21
- Country
- United States
- Brand
- Sarnova HC
- Product
- Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT
- Classification
- Class II
- Units
- US Nationwide distribution in the states of IA, IL, IN, KY, MI, MN, MO, ND,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Sarnova HC recalls
- 2024-03-27
Sarnova HC, Llc recalls Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number:…
Endotracheal Tube Holder included in certain kits is not compatible with a nasal intubation procedure, leaving practitioners without the necessary means to secure the inserted endotracheal tube.
- 2024-01-24
Sarnova HC, Llc recalls Curaplex Cricothyrotomy Field Kit with Instruments, Kwik Cric MVP, 6.0mm, Item Number 351631i-A. The kit provides healthcare professionals…
It was determined that the Endotracheal Tube Holder included in certain kits is not compatible with a cricothyrotomy procedure, leaving practitioners without the necessary means to secure the inserted endotracheal tube.
USOther drugs & medical recalls in the United States
- 2026-10-21
INTEGRATED MEDCRAFT LLC recalls FORWARD Gunshot Wound Kit; Model: AFT-GSW;
Subrecall of a kitted device from SafeGuard Medical due to internal testing identified an issue affecting the device's sterile pad, potentially causing the sterile pad to degrade over time. The degradation may cause…
FDA · DeviceINTEGRATED MEDCRAFT LLCUS Nationwide distribution in the states of GA, VA.Official notice →SI-BONE, Inc. recalls iFuse TORQ Implant System Model/Catalog Number: 10055T(10x55mm), 10060T(10x60mm), 10065T(10x65mm), 10080T(10x55mm), 11580T(11.5x80mm)
The pelvic fixation screws failed to meet acceptance criteria for tube packaging seal integrity testing; therefore, sterility assurance cannot be ensured.
FDA · DeviceSI-BONE, Inc.US Nationwide distribution in the states of FL, GA, HI, NC, OH, PA, SD, TX, VA.Official notice →Ferno-Washington Inc recalls Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X2, Item No. 0015816 and PowerX2…
Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to the system not operating in powered mode, or exhibiting reduced…
FDA · DeviceFerno-Washington IncWorldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO,…Official notice →Boston Scientific Corporation recalls NaviFlex LW Pusher; Advx Panc. Stent 4/5F; Material Number (UPN): M00535030;
Device was incorrectly manufactured with a guidewire exit port (referred to in the IFU as the RX port), which is not a design feature associated with this device configuration.
FDA · DeviceBoston Scientific CorporationUS Nationwide distribution in the states of AL, CA, FL, GA, IL, IN, KY, MD,…Official notice →Neuronetics, Inc. recalls NeuroStar Advanced Therapy System. Contains the NeuroStar HP Coil Assembly Part Number 81-01000-200. Affects the below NeuroStar Advanced…
Cables are not in conformance with the product specifications required in the production of the HP Coil Assembly.
FDA · DeviceNeuronetics, Inc.Worldwide distribution - US Nationwide and the countries of Japan and South…Official notice →Cadwell Industries Inc recalls Brand Name: IOMAX Product Name: IOMAX Cortical Module Model/Catalog Number: 190296-200 UDI-DI code: 00840067100653 Product Description:…
Stimulator device contains a defective printed circuit board assembly (PCBA) that may cause the device to unintentionally deliver electrical stimulation to the patient, or allow an unintended electrical current to…
FDA · DeviceCadwell Industries IncWorldwide - US Nationwide distribution in the state of TN and the countries of…Official notice →