Ansell Healthcare Products LLC recalls Gammex Non-Latex PI Green PI-KARE Skin-friendly PI Technology polyisoprene surgical gloves 7 1/2
Transport company failed to stop at the border for required FDA inspection.
Read the official notice →- Date
- 2022-04-06
- Country
- United States
- Brand
- Ansell Healthcare Products
- Product
- Gammex Non-Latex PI Green PI-KARE Skin-friendly PI Technology polyisoprene surgical gloves 7 1/2
- Classification
- Class II
- Units
- U.S.: AZ, CA, NV, TX, UT and WA O.U.S.: None
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Ansell Healthcare Products recalls
- 2023-10-18
US
Ansell Healthcare Products LLC recalls NOVAPLUS GAMMEX NON-LATEX PI GREEN Surgical gloves, REF: V20685255 through V20685290
Some surgical glove sterile pouches were not completely sealed.
FDA · DeviceAnsell Healthcare Products LLCWorldwide - US Nationwide distribution in the states of IN, OH, NY, VA, IL,…Official notice →
Other drugs & medical recalls in the United States
- 2022-04-06
US
Microbiologics Inc recalls Pneumonia (33 Targets) Control Panel, unassayed quality control material, containing: Positive Control 1 - Semi-Quantitative Bacteria…
Shelf-life for the 8244 Pneumonia (33 Targets) Control Panel determined to be 6 months instead of 18 months.
FDA · DeviceMicrobiologics IncUS distribution to Alabama, Georgia, Illinois, Montana, Pennsylvania,…Official notice →US
Howmedica Osteonics Corp. recalls Biolox delta Ceramic V40 Femoral Head 32/ +4.0mm Catalog Number: 6570-0-232
Potential product mix where the size and/or offset of the Biolox delta Ceramic V40 Femoral Head inside the package does not match the package labeling
FDA · DeviceHowmedica Osteonics Corp.Worldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice →US
Siemens Medical Solutions USA, Inc recalls Ysiosystem with VC10 software version, Model Number 10281013. Radiographic system
Siemens Healthineers has identified a software error in previous software version VB10 for the Ysio fully automated system. The unit may process incorrect internal values for the position of its ceiling tube stand. If…
US
ROi CPS LLC recalls Regard Custom Procedure Kits containing BD Luer Lok Access Devices
Recalled devices were packaged in convenience kits.
US
Meridian Bioscience Inc recalls Revogene, For In Vitro Diagnostic use in performing nucleic acid testing in clinical laboratories. Meridian branded Revogene: Catalog…
The photomultiplier tube, may have compromised functionality in some instruments. As a result, the user is likely to observe an increase in false-positive or indeterminate results.
FDA · DeviceMeridian Bioscience IncWorldwide distribution - US Nationwide distribution in the states of AK, AL,…Official notice →US
Edwards Lifesciences, LLC recalls FORE-SIGHT ELITE Absolute Tissue Oximeter, REF: 01-06-3000, Contents: Monitor 1 EA., Accessory Kit 1 EA.
The StO2 values may be inaccurately low when using either the FORE-SIGHT ELITE Tissue Oximeter Module or the FORE-SIGHT ELITE Absolute Tissue Oximeter Monitor with the Fore-Sight Elite large sensor in certain somatic…
FDA · DeviceEdwards Lifesciences, LLCWorldwide distribution - US Nationwide distribution in the states of AK, AL,…Official notice →