SVS LLC recalls Non-sterile, single use, disposable gloves intended for medical purposes to be worn on the hands of examiners to prevent contamination…
Firm received complaints regarding skin irritation when using the gloves, disintegration of the gloves when used with certain cleaning solutions, and mislabeled products (e.g., outer box indicating one size, but inner…
Read the official notice →- Date
- 2024-07-17
- Country
- United States
- Brand
- SVS LLC
- Product
- Non-sterile, single use, disposable gloves intended for medical purposes to be worn on the hands of examiners to prevent contamination…
- Classification
- Class II
- Units
- US Nationwide distribution in the states of MI, NE, FL, GA, PA, AR, CO, and NY.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2024-07-17
US
Echonous Inc recalls Kosmos on iOS impacting iOS, Model Numbers: P007639, P007944, software is part of a general-purpose diagnostic ultrasound system.
Ultrasound system has a bug in affected iOS software, which after DICOM export, can cause inaccuracy in postprocessed measurements done in 3rd party software, such as PACS or other post-processing software, which may…
FDA · DeviceEchonous IncUS: ID, TX, WI, KS, IL, GA, MI, CA, OH, FL, AK, UT, MD, NY, NV, CO, ND, WA,…Official notice →US
Zoll Medical Corporation recalls ZOLL Powerheart G5 AED, Semi-Automatic, G5Sxxx Family -Automated external defibrillator (AED) is designed for treating life-threatening…
G5 Semi-Automatic AED is shipped, with a protective film over its front panel, to protect the screen and shock button from cosmetic damage during shipping. It has come to our attention that customers may not be…
FDA · DeviceZoll Medical CorporationNationwide including PR. Foreign: AU BM CA CH DE DK ES FR GB HK HU ID IE IL IT…Official notice →US
Baxter Healthcare Corporation recalls Welch Allyn CP150 Electrocardiograph with Spirometry Option, Product Code: CP150A-1ENB. The Electrocardiograph is one of the tools…
During manufacturing, the step to install an Electromagnetic Interference (EMI) Absorber was omitted. The purpose of the EMI absorber is to prevent EMI leakage that might potentially affect other devices in the…
US
Preat Corp recalls 9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixture…
Due to incorrect milled titanium abutment being packaged and labeled.
US
GE Vingmed Ultrasound As recalls GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW
GE HealthCare has become aware of an issue with certain Vivid ultrasound systems where, due to a slow DICOM Worklist response time, incorrect patient name and demographics can be displayed on the ultrasound scanner…
US
Baxter Healthcare Corporation recalls Trulight 5000/3000 Surgical Light, model numbers: a) 4038210 (Duo Surgical Lights}; b) 4038310 (Trio/Quad Surgical Lights)
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products listed below. Specific VidiaPort and…