All recalls8,424 total
Contains statement does not declare Crab and Pollock
Contains statement does not declare Salmon
Contains statement does not declare Almond
Contains statement does not declare Pistachio
Contains statement does not declare Hazelnut
Contains statement does not declare pecan.
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
Contains statement does not declare Tuna
Contains statement does not declare Crab
Contains statement does not declare Shrimp.
Contains statement does not declare Almond
Contains statement does not declare Tilapia
Contains statement does not declare Almond.
Contains statement does not declare Anchovy
Contains statement does not declare Shrimp.
Contains statement does not declare Almond
Contains statement does not declare Pistachio
Contains statement does not declare Walnut
Contains statement does not declare Almond
Contains statement does not declare Walnut
Contains statement does not declare Walnut
Contains statement does not declare Salmon
Contains statement does not declare Almond
Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.
Contains statement does not declare Shrimp.
Contains statement does not declare Anchovy
Contains statement does not declare Cashew
Contains statement does not declare Pistachio
Contains statement does not declare Crab and Pollock
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huon Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.
It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being shipped to your facility. There is a potential risk of electrical shock due to the device s safety testing being unverifiable.
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huon Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut down the pump unless it is reconnected to AC mains power.
Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components that may not be apparent or readily visible and the devices therefore remained in service. More specifically, drops or jarring on a hard surface can cause the touchscreen input cable to loosen, resulting in unintended touchscreen behavior on the LVP, including random screen touches and/or lack of screen responsiveness to user input. Under the reported failure condition, unintended touch inputs may register at arbitrary screen locations without user interaction. These inputs occur intermittently and without a predictable pattern.
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huon Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.
potential presence of Salmonella
Products were made with recalled California Dairies milk powder due to Salmonella.
potential presence of Salmonella
Product was manufactured and distributed without the benefit of an approved food establishment inspection and the required regulatory safety parameters could not be verified.
potential presence of Salmonella
potential presence of Salmonella
potential presence of Salmonella
Product may be contaminated with Salmonella.
Products were made with recalled California Dairies milk powder due to Salmonella.
Products were made with recalled California Dairies milk powder due to Salmonella.