North American Rescue LLC. recalls AIDBAGs are first aid kits of convenience composed of individually labeled devices designed as specialty first aid kits designed for…
Kits contain the McKesson TRUE Metrix PRO Professional Monitoring Blood Glucose System that has been recalled for an issue with the software design of the E-5 Error Code where the meter displays an E-5 error code for a…
Read the official notice →- Date
- 2026-05-06
- Country
- United States
- Brand
- North American Rescue
- Product
- AIDBAGs are first aid kits of convenience composed of individually labeled devices designed as specialty first aid kits designed for the…
- Classification
- Class I
- Units
- US: CA, WA
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 North American Rescue recalls
- 2025-10-08
USNorth American Rescue LLC. recalls JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088, a component inside kits: KIT, TCCC Training- Complete (Modules 1-3), REF:…
Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the structural integrity of the device and device performance during use.
FDA · DeviceNorth American Rescue LLC.Worldwide - US Nationwide distribution in the states of SC, OK, ID, KY, VA,…Official notice →
Other drugs & medical recalls in the United States
- 2026-05-06
- US
Advanced Bionics, LLC recalls Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110; CI-5501-120;…
The non-tamperproof battery door supplied with the sound processor fails to conform to IEC 60601-1-11:2015 by not requiring the use of a tool to replace the button/coin cell battery.
FDA · DeviceAdvanced Bionics, LLCWorldwide - U.S Nationwide distribution including in the state of AK, AL, AR,…Official notice → - US
Hologic, Inc recalls Brand Name: Genius" Review Station Product Name: Genius" Review Station Display (Barco Monitor) Model/Catalog Number: CMP-01669 Software…
It was identified that certain devices were being operated outside the validated and FDA-cleared display configuration due to user modification of the manufacturer-installed settings. Modifications included disabling…
FDA · DeviceHologic, IncWorldwide distribution - US Nationwide and the countries of Asia Pacific,…Official notice → - US
Medtronic, Inc. recalls Medtronic Sphere-9 Catheter, Model Number AFR-00001; catheter, percutaneous, cardiac ablation, for treatment of atrial flutter.
Ventricular fibrillation (VF) occurred during radiofrequency (RF) therapy with the Medtronic Sphere-9 catheter in patients who have a Biotronik Implantable Cardioverter Defibrillator (ICD) or Biotronik Cardiac…
- US
Zimmer, Inc. recalls Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and Spatula Model/Catalog Number: 00-5049-011-00 Software…
Ten complaints have been received identifying issues at the time of use related to the package seal, including incomplete seals, wrinkles in the seals or peeling seals. Compromised sterile barrier may lead to…
FDA · DeviceZimmer, Inc.US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, FL,…Official notice → - US
Clinical Innovations, LLC recalls Brand Name: Kiwi Omni Vacuum Delivery System Product Name: Kiwi Omni Vacuum Delivery System Model/Catalog Number: VAC-6000MT Product…
Due to complaints of device breakage at the traction force gauge to handle joint.
FDA · DeviceClinical Innovations, LLCWorldwide - U.S. Nationwide distribution including in the states of AK, AR,…Official notice → - US
Milestone S.R.L. recalls VACUUM BAG SU LARGE, Non-sterile specimen container, Model/Catalog Number: 68409SS
There is a possibility of reagent leakage from the specimen container.
FDA · DeviceMilestone S.R.L.Worldwide distribution - US Nationwide and the countries of Canada, Chile,…Official notice →