Wilton Chocolate decorator icing stiff consistency 16 oz plastic tub retail unit 6 or 12 retail units per wholesale unit
Wilton Brands
🍎 Food Class I - Dangerous
Mold
All Recalls
95,050 total recalls in our database
💊 Drugs Class I - Dangerous
Lack of Assurance of Sterility: Bags have the potential to leak.
💊 Drugs Class I - Dangerous
Labeling: Missing label; Product complaints reported missing bottle label.
💊 Drugs Class I - Dangerous
Lack of Assurance of Sterility: Bags have the potential to leak.
💊 Drugs Class I - Dangerous
Presence of Particulate Matter; glass particulates
ElectroMist product codes: 36-3310-25 - Product Usage: Electrode conductivity spray solution.
Pharmaceutical Innovations
🏥 Medical Devices Class I - Dangerous
Potential for failed stability antimicrobial effectiveness testing.
🏥 Medical Devices Class I - Dangerous
The products do not have sufficient data to support the labeled shelf life of 10 years.
🏥 Medical Devices Class I - Dangerous
Compatibility issue between the software and Microsoft updates to Windows 7, 8, and 10. The compatibility issue causes the software to be unusable which could result in a delay of reporting results.
Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only), Item Number 595510
Zimmer Biomet
🏥 Medical Devices Class I - Dangerous
Lack of an adequate sterilization validation.
🏥 Medical Devices Class I - Dangerous
Calibration failures with Std.E, Sens.E, or Dup.E error due to atypical reaction kinetics and quality control failures have occurred due to contamination of R1 reagent with R3 reagent.
Alpha Conducting solution product codes: 3310-25 ASCR - Product Usage: Electrode Conductivity Spray Solution.
Pharmaceutical Innovations
🏥 Medical Devices Class I - Dangerous
Potential for failed stability antimicrobial effectiveness testing.
A-CIFT SoloFuse Fixed Angle Driver, Model Number 13-32101-01 (Component Part Numbers 14-32107-01 and 14-32106)
SpineFrontier
🏥 Medical Devices Class I - Dangerous
There is a potential for the driver to bind up when attempting to advance the intervertebral body fixation screw.
DeRoyal THE RESOURCE GROUP, CRANI PACK, REF 89-9211.07 custom surgical pack
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
Custom surgical packs are being recalled because it contains Cardinal Health Blunt Cannulas which were recalled due to a manufacturing defect in the cartridge component which could compromise the sterility barrier of the product.
🏥 Medical Devices Class I - Dangerous
The product may not meet sterility requirements. Product labeled as sterile, however all units do not appear to meet sterility requirements.
The Anti-Fog Solution may not defog properly due to a degradation in the chemical properties.
🏥 Medical Devices Class I - Dangerous
Potential for a transducer mis-alignment in certain transvaginal probes.
🏥 Medical Devices Class I - Dangerous
If battery maintenance is not performed appropriately, the battery may provide less than the minimum run time of operating power. Revised labeling and training are being provided.
🏥 Medical Devices Class I - Dangerous
If battery maintenance is not performed appropriately, the battery may provide less than the minimum run time of operating power. Revised labeling and training are being offered.
🏥 Medical Devices Class I - Dangerous
If battery maintenance is not performed per instructions, the battery may provide less than the minimum run time of operating power.
ElectroMist product codes: 36-3310-60 - Product Usage: Electrode Conductivity Spray Solution.
Pharmaceutical Innovations
🏥 Medical Devices Class I - Dangerous
Potential for failed stability antimicrobial effectiveness testing.