Neurovision Medical Products Inc recalls Brand Name: Hummingbird Product Name: Stimulated EMG Kit with Hummingbird - Model/Catalog Number: REF I-D-BMF90, 1 Single-Use…
Product packaging contains the wrong part number and kit contents.
Read the official notice →- Date
- 2025-07-16
- Country
- United States
- Brand
- Neurovision Medical Products
- Product
- Brand Name: Hummingbird Product Name: Stimulated EMG Kit with Hummingbird - Model/Catalog Number: REF I-D-BMF90, 1 Single-Use Bipolar…
- Classification
- Class II
- Units
- US distribution to CA only
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Neurovision Medical Products recalls
- 2024-09-04
US
Neurovision Medical Products Inc recalls Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO
mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Other drugs & medical recalls in the United States
- 2025-07-16
US
Preat Corp recalls Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx Only
Due to manufacturing error, digital analog rotational feature is 180 degrees off.
FDA · DevicePreat CorpUS Nationwide distribution in the states of AL, CA, FL, GA, KY, MD, MN, NY,…Official notice →US
Boston Scientific Corporation recalls Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F 63CM 45DEG TF85-32-63-55 TORFLEX 8.5F 63CM 55DEG Used…
Potential for hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. Issue could potentially lead to systemic infection and sepsis in worst case scenario. Potential punctures may…
FDA · DeviceBoston Scientific CorporationWorldwide distribution - US Nationwide and the countries of Canada, Hong Kong,…Official notice →US
Medtronic Navigation, Inc.-Boxborough recalls O-arm O2 Imaging System. Mobile X-Ray System.
A mechanical component that supports the O2 gantry to the support structure in affected devices may have been damaged during manufacture.
FDA · DeviceMedtronic Navigation, Inc.-BoxboroughUS Nationwide distribution in the states of IN, MN, MS.Official notice →US
Canary Medical, Inc. recalls Brand Name: Canturio¿ Smart Extension Product Name: CSE Implant Model/Catalog Number: 43-5570-030-14 Product Description: Tibial stem…
Due to labeling error. Product incorrectly labeled.
US
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING recalls Infinia, Infinia Hawkeye, Infinia II, Infinia II Hawkeye 4 Nuclear Medicine system
Unintended radial detector motion may occur during patient setup or during patient scan if system does not have correct version of gantry software installed. Unintended detector motion may result in life-threatening…
FDA · DeviceGE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGINGWorldwide - US Nationwide distribution.Official notice →US
STRATASYS LTD recalls TrueDent Clear, TDM 100, Model No. OBJ-09164 Light-curable methacrylate-based resin that enables fabrication of dental appliances
Customers unable to use cartridges due to formatting error in expiration date which leads to switching the day with the month. Or, the system will not recognize that a resin is expired and will not prevent the user…
FDA · DeviceSTRATASYS LTDUS Nationwide distribution including in the states of Arizona, Arkansas,…Official notice →